Canonical Allele Identifier: CA2262104671

Gene: MAPT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46018483_46018489delinsCCAATCT , CM000679.2:g.46018483_46018489delinsCCAATCT	GRCh38
NC_000017.10:g.44095849_44095855delinsCCAATCT , CM000679.1:g.44095849_44095855delinsCCAATCT	GRCh37
NC_000017.9:g.41451696_41451702delinsCCAATCT	NCBI36
NG_007398.1:g.129073_129079delinsCCAATCT
NG_007398.2:g.129021_129027delinsCCAATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.911-135_911-129delinsCCAATCT	ENSP00000413056.2:n.911-135_911-129delinsCCAATCT
ENST00000703922.1:c.911-135_911-129delinsCCAATCT	ENSP00000515557.1:n.911-135_911-129delinsCCAATCT
ENST00000703923.1:c.824-135_824-129delinsCCAATCT	ENSP00000515558.1:n.824-135_824-129delinsCCAATCT
ENST00000703924.1:c.911-135_911-129delinsCCAATCT	ENSP00000515559.1:n.911-135_911-129delinsCCAATCT
ENST00000703978.1:c.998-135_998-129delinsCCAATCT	ENSP00000515600.1:n.998-135_998-129delinsCCAATCT
ENST00000703979.1:n.769-135_769-129delinsCCAATCT
ENST00000703980.1:n.224-135_224-129delinsCCAATCT
ENST00000703981.1:n.182-135_182-129delinsCCAATCT
ENST00000703982.1:n.281_287delinsCCAATCT
ENST00000262410.10:c.2174-135_2174-129delinsCCAATCT MANE Select	ENSP00000262410.6:n.2174-135_2174-129delinsCCAATCT
ENST00000344290.10:c.1883-135_1883-129delinsCCAATCT	ENSP00000340820.6:n.1883-135_1883-129delinsCCAATCT
ENST00000351559.10:c.998-135_998-129delinsCCAATCT	ENSP00000303214.7:n.998-135_998-129delinsCCAATCT
ENST00000535772.6:c.818-135_818-129delinsCCAATCT	ENSP00000443028.2:n.818-135_818-129delinsCCAATCT
ENST00000680542.1:c.911-135_911-129delinsCCAATCT	ENSP00000505258.1:n.911-135_911-129delinsCCAATCT
ENST00000680674.1:c.947-135_947-129delinsCCAATCT	ENSP00000505478.1:n.947-135_947-129delinsCCAATCT
ENST00000262410.9:c.1949-135_1949-129delinsCCAATCT	ENSP00000262410.5:n.1949-135_1949-129delinsCCAATCT
ENST00000334239.12:c.731-135_731-129delinsCCAATCT	ENSP00000334886.8:n.731-135_731-129delinsCCAATCT
ENST00000340799.9:c.911-135_911-129delinsCCAATCT	ENSP00000340438.5:n.911-135_911-129delinsCCAATCT
ENST00000344290.9:c.2003-135_2003-129delinsCCAATCT	ENSP00000340820.5:n.2003-135_2003-129delinsCCAATCT
ENST00000351559.9:c.998-135_998-129delinsCCAATCT	ENSP00000303214.7:n.998-135_998-129delinsCCAATCT
ENST00000415613.6:c.2003-135_2003-129delinsCCAATCT	ENSP00000410838.2:n.2003-135_2003-129delinsCCAATCT
ENST00000420682.6:c.911-135_911-129delinsCCAATCT	ENSP00000413056.2:n.911-135_911-129delinsCCAATCT
ENST00000431008.7:c.905-135_905-129delinsCCAATCT	ENSP00000389250.3:n.905-135_905-129delinsCCAATCT
ENST00000446361.7:c.824-135_824-129delinsCCAATCT	ENSP00000408975.3:n.824-135_824-129delinsCCAATCT
ENST00000535772.5:c.905-135_905-129delinsCCAATCT	ENSP00000443028.1:n.905-135_905-129delinsCCAATCT
ENST00000570299.5:n.777-135_777-129delinsCCAATCT
ENST00000571987.5:c.1949-135_1949-129delinsCCAATCT	ENSP00000458742.1:n.1949-135_1949-129delinsCCAATCT
ENST00000574436.5:c.998-135_998-129delinsCCAATCT	ENSP00000460965.1:n.998-135_998-129delinsCCAATCT
ENST00000576518.1:n.6190-135_6190-129delinsCCAATCT
NM_001123066.3:c.2003-135_2003-129delinsCCAATCT	NP_001116538.2:n.2003-135_2003-129delinsCCAATCT
NM_001123067.3:c.911-135_911-129delinsCCAATCT	NP_001116539.1:n.911-135_911-129delinsCCAATCT
NM_001203251.1:c.818-135_818-129delinsCCAATCT	NP_001190180.1:n.818-135_818-129delinsCCAATCT
NM_001203252.1:c.905-135_905-129delinsCCAATCT	NP_001190181.1:n.905-135_905-129delinsCCAATCT
NM_005910.5:c.998-135_998-129delinsCCAATCT	NP_005901.2:n.998-135_998-129delinsCCAATCT
NM_016834.4:c.824-135_824-129delinsCCAATCT	NP_058518.1:n.824-135_824-129delinsCCAATCT
NM_016835.4:c.1949-135_1949-129delinsCCAATCT	NP_058519.3:n.1949-135_1949-129delinsCCAATCT
NM_016841.4:c.731-135_731-129delinsCCAATCT	NP_058525.1:n.731-135_731-129delinsCCAATCT
XM_005257362.3:c.2261-135_2261-129delinsCCAATCT	XP_005257419.1:n.2261-135_2261-129delinsCCAATCT
XM_005257364.3:c.2174-135_2174-129delinsCCAATCT	XP_005257421.1:n.2174-135_2174-129delinsCCAATCT
XM_005257365.3:c.2168-135_2168-129delinsCCAATCT	XP_005257422.1:n.2168-135_2168-129delinsCCAATCT
XM_005257366.2:c.2087-135_2087-129delinsCCAATCT	XP_005257423.1:n.2087-135_2087-129delinsCCAATCT
XM_005257367.3:c.2063-135_2063-129delinsCCAATCT	XP_005257424.1:n.2063-135_2063-129delinsCCAATCT
XM_005257368.3:c.1970-135_1970-129delinsCCAATCT	XP_005257425.1:n.1970-135_1970-129delinsCCAATCT
XM_005257369.3:c.1196-135_1196-129delinsCCAATCT	XP_005257426.1:n.1196-135_1196-129delinsCCAATCT
XM_005257370.3:c.1109-135_1109-129delinsCCAATCT	XP_005257427.1:n.1109-135_1109-129delinsCCAATCT
XM_005257371.3:c.1022-135_1022-129delinsCCAATCT	XP_005257428.1:n.1022-135_1022-129delinsCCAATCT
XM_005257362.4:c.2261-135_2261-129delinsCCAATCT	XP_005257419.1:n.2261-135_2261-129delinsCCAATCT
XM_005257364.4:c.2174-135_2174-129delinsCCAATCT	XP_005257421.1:n.2174-135_2174-129delinsCCAATCT
XM_005257365.4:c.2168-135_2168-129delinsCCAATCT	XP_005257422.1:n.2168-135_2168-129delinsCCAATCT
XM_005257366.3:c.2087-135_2087-129delinsCCAATCT	XP_005257423.1:n.2087-135_2087-129delinsCCAATCT
XM_005257367.4:c.2063-135_2063-129delinsCCAATCT	XP_005257424.1:n.2063-135_2063-129delinsCCAATCT
XM_005257368.4:c.1970-135_1970-129delinsCCAATCT	XP_005257425.1:n.1970-135_1970-129delinsCCAATCT
XM_005257369.4:c.1196-135_1196-129delinsCCAATCT	XP_005257426.1:n.1196-135_1196-129delinsCCAATCT
XM_005257370.4:c.1109-135_1109-129delinsCCAATCT	XP_005257427.1:n.1109-135_1109-129delinsCCAATCT
XM_005257371.4:c.1022-135_1022-129delinsCCAATCT	XP_005257428.1:n.1022-135_1022-129delinsCCAATCT
NM_001203251.2:c.818-135_818-129delinsCCAATCT	NP_001190180.1:n.818-135_818-129delinsCCAATCT
NM_001377265.1:c.2174-135_2174-129delinsCCAATCT MANE Select	NP_001364194.1:n.2174-135_2174-129delinsCCAATCT
NM_001377266.1:c.1883-135_1883-129delinsCCAATCT	NP_001364195.1:n.1883-135_1883-129delinsCCAATCT
NM_001377267.1:c.771+4205_771+4211delinsCCAATCT	NP_001364196.1:n.771+4205_771+4211delinsCCAATCT
NM_001377268.1:c.731-135_731-129delinsCCAATCT	NP_001364197.1:n.731-135_731-129delinsCCAATCT
NM_016834.5:c.824-135_824-129delinsCCAATCT	NP_058518.1:n.824-135_824-129delinsCCAATCT
NM_016841.5:c.731-135_731-129delinsCCAATCT	NP_058525.1:n.731-135_731-129delinsCCAATCT
NR_165166.1:n.829-135_829-129delinsCCAATCT
NM_001123066.4:c.2003-135_2003-129delinsCCAATCT	NP_001116538.2:n.2003-135_2003-129delinsCCAATCT
NM_001123067.4:c.911-135_911-129delinsCCAATCT	NP_001116539.1:n.911-135_911-129delinsCCAATCT
NM_001203252.2:c.905-135_905-129delinsCCAATCT	NP_001190181.1:n.905-135_905-129delinsCCAATCT
NM_005910.6:c.998-135_998-129delinsCCAATCT	NP_005901.2:n.998-135_998-129delinsCCAATCT
NM_016835.5:c.1949-135_1949-129delinsCCAATCT	NP_058519.3:n.1949-135_1949-129delinsCCAATCT