Canonical Allele Identifier: CA772442444

Gene: MAPT

Linked Data

• dbSNP Id: rs1273740879
• MyVariant Identifiers: chr17:g.44095814_44095815insTGTT (hg19) ; chr17:g.46018448_46018449insTGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46018451_46018452insTTGT , CM000679.2:g.46018451_46018452insTTGT	GRCh38
NC_000017.10:g.44095817_44095818insTTGT , CM000679.1:g.44095817_44095818insTTGT	GRCh37
NC_000017.9:g.41451664_41451665insTTGT	NCBI36
NG_007398.1:g.129041_129042insTTGT
NG_007398.2:g.128989_128990insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.911-167_911-166insTTGT	ENSP00000413056.2:n.911-167_911-166insTTGT
ENST00000703922.1:c.911-167_911-166insTTGT	ENSP00000515557.1:n.911-167_911-166insTTGT
ENST00000703923.1:c.824-167_824-166insTTGT	ENSP00000515558.1:n.824-167_824-166insTTGT
ENST00000703924.1:c.911-167_911-166insTTGT	ENSP00000515559.1:n.911-167_911-166insTTGT
ENST00000703978.1:c.998-167_998-166insTTGT	ENSP00000515600.1:n.998-167_998-166insTTGT
ENST00000703979.1:n.769-167_769-166insTTGT
ENST00000703980.1:n.224-167_224-166insTTGT
ENST00000703981.1:n.182-167_182-166insTTGT
ENST00000703982.1:n.249_250insTTGT
ENST00000262410.10:c.2174-167_2174-166insTTGT MANE Select	ENSP00000262410.6:n.2174-167_2174-166insTTGT
ENST00000344290.10:c.1883-167_1883-166insTTGT	ENSP00000340820.6:n.1883-167_1883-166insTTGT
ENST00000351559.10:c.998-167_998-166insTTGT	ENSP00000303214.7:n.998-167_998-166insTTGT
ENST00000535772.6:c.818-167_818-166insTTGT	ENSP00000443028.2:n.818-167_818-166insTTGT
ENST00000680542.1:c.911-167_911-166insTTGT	ENSP00000505258.1:n.911-167_911-166insTTGT
ENST00000680674.1:c.947-167_947-166insTTGT	ENSP00000505478.1:n.947-167_947-166insTTGT
ENST00000262410.9:c.1949-167_1949-166insTTGT	ENSP00000262410.5:n.1949-167_1949-166insTTGT
ENST00000334239.12:c.731-167_731-166insTTGT	ENSP00000334886.8:n.731-167_731-166insTTGT
ENST00000340799.9:c.911-167_911-166insTTGT	ENSP00000340438.5:n.911-167_911-166insTTGT
ENST00000344290.9:c.2003-167_2003-166insTTGT	ENSP00000340820.5:n.2003-167_2003-166insTTGT
ENST00000351559.9:c.998-167_998-166insTTGT	ENSP00000303214.7:n.998-167_998-166insTTGT
ENST00000415613.6:c.2003-167_2003-166insTTGT	ENSP00000410838.2:n.2003-167_2003-166insTTGT
ENST00000420682.6:c.911-167_911-166insTTGT	ENSP00000413056.2:n.911-167_911-166insTTGT
ENST00000431008.7:c.905-167_905-166insTTGT	ENSP00000389250.3:n.905-167_905-166insTTGT
ENST00000446361.7:c.824-167_824-166insTTGT	ENSP00000408975.3:n.824-167_824-166insTTGT
ENST00000535772.5:c.905-167_905-166insTTGT	ENSP00000443028.1:n.905-167_905-166insTTGT
ENST00000570299.5:n.777-167_777-166insTTGT
ENST00000571987.5:c.1949-167_1949-166insTTGT	ENSP00000458742.1:n.1949-167_1949-166insTTGT
ENST00000574436.5:c.998-167_998-166insTTGT	ENSP00000460965.1:n.998-167_998-166insTTGT
ENST00000576518.1:n.6190-167_6190-166insTTGT
NM_001123066.3:c.2003-167_2003-166insTTGT	NP_001116538.2:n.2003-167_2003-166insTTGT
NM_001123067.3:c.911-167_911-166insTTGT	NP_001116539.1:n.911-167_911-166insTTGT
NM_001203251.1:c.818-167_818-166insTTGT	NP_001190180.1:n.818-167_818-166insTTGT
NM_001203252.1:c.905-167_905-166insTTGT	NP_001190181.1:n.905-167_905-166insTTGT
NM_005910.5:c.998-167_998-166insTTGT	NP_005901.2:n.998-167_998-166insTTGT
NM_016834.4:c.824-167_824-166insTTGT	NP_058518.1:n.824-167_824-166insTTGT
NM_016835.4:c.1949-167_1949-166insTTGT	NP_058519.3:n.1949-167_1949-166insTTGT
NM_016841.4:c.731-167_731-166insTTGT	NP_058525.1:n.731-167_731-166insTTGT
XM_005257362.3:c.2261-167_2261-166insTTGT	XP_005257419.1:n.2261-167_2261-166insTTGT
XM_005257364.3:c.2174-167_2174-166insTTGT	XP_005257421.1:n.2174-167_2174-166insTTGT
XM_005257365.3:c.2168-167_2168-166insTTGT	XP_005257422.1:n.2168-167_2168-166insTTGT
XM_005257366.2:c.2087-167_2087-166insTTGT	XP_005257423.1:n.2087-167_2087-166insTTGT
XM_005257367.3:c.2063-167_2063-166insTTGT	XP_005257424.1:n.2063-167_2063-166insTTGT
XM_005257368.3:c.1970-167_1970-166insTTGT	XP_005257425.1:n.1970-167_1970-166insTTGT
XM_005257369.3:c.1196-167_1196-166insTTGT	XP_005257426.1:n.1196-167_1196-166insTTGT
XM_005257370.3:c.1109-167_1109-166insTTGT	XP_005257427.1:n.1109-167_1109-166insTTGT
XM_005257371.3:c.1022-167_1022-166insTTGT	XP_005257428.1:n.1022-167_1022-166insTTGT
XM_005257362.4:c.2261-167_2261-166insTTGT	XP_005257419.1:n.2261-167_2261-166insTTGT
XM_005257364.4:c.2174-167_2174-166insTTGT	XP_005257421.1:n.2174-167_2174-166insTTGT
XM_005257365.4:c.2168-167_2168-166insTTGT	XP_005257422.1:n.2168-167_2168-166insTTGT
XM_005257366.3:c.2087-167_2087-166insTTGT	XP_005257423.1:n.2087-167_2087-166insTTGT
XM_005257367.4:c.2063-167_2063-166insTTGT	XP_005257424.1:n.2063-167_2063-166insTTGT
XM_005257368.4:c.1970-167_1970-166insTTGT	XP_005257425.1:n.1970-167_1970-166insTTGT
XM_005257369.4:c.1196-167_1196-166insTTGT	XP_005257426.1:n.1196-167_1196-166insTTGT
XM_005257370.4:c.1109-167_1109-166insTTGT	XP_005257427.1:n.1109-167_1109-166insTTGT
XM_005257371.4:c.1022-167_1022-166insTTGT	XP_005257428.1:n.1022-167_1022-166insTTGT
NM_001203251.2:c.818-167_818-166insTTGT	NP_001190180.1:n.818-167_818-166insTTGT
NM_001377265.1:c.2174-167_2174-166insTTGT MANE Select	NP_001364194.1:n.2174-167_2174-166insTTGT
NM_001377266.1:c.1883-167_1883-166insTTGT	NP_001364195.1:n.1883-167_1883-166insTTGT
NM_001377267.1:c.771+4173_771+4174insTTGT	NP_001364196.1:n.771+4173_771+4174insTTGT
NM_001377268.1:c.731-167_731-166insTTGT	NP_001364197.1:n.731-167_731-166insTTGT
NM_016834.5:c.824-167_824-166insTTGT	NP_058518.1:n.824-167_824-166insTTGT
NM_016841.5:c.731-167_731-166insTTGT	NP_058525.1:n.731-167_731-166insTTGT
NR_165166.1:n.829-167_829-166insTTGT
NM_001123066.4:c.2003-167_2003-166insTTGT	NP_001116538.2:n.2003-167_2003-166insTTGT
NM_001123067.4:c.911-167_911-166insTTGT	NP_001116539.1:n.911-167_911-166insTTGT
NM_001203252.2:c.905-167_905-166insTTGT	NP_001190181.1:n.905-167_905-166insTTGT
NM_005910.6:c.998-167_998-166insTTGT	NP_005901.2:n.998-167_998-166insTTGT
NM_016835.5:c.1949-167_1949-166insTTGT	NP_058519.3:n.1949-167_1949-166insTTGT