Canonical Allele Identifier: CA2262104718
Gene: MAPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46018598_46018600delinsTTG , CM000679.2:g.46018598_46018600delinsTTG GRCh38
NC_000017.10:g.44095964_44095966delinsTTG , CM000679.1:g.44095964_44095966delinsTTG GRCh37
NC_000017.9:g.41451811_41451813delinsTTG NCBI36
NG_007398.1:g.129188_129190delinsTTG
NG_007398.2:g.129136_129138delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000420682.7:c.911-20_911-18delinsTTG ENSP00000413056.2:n.911-20_911-18delinsTTG
ENST00000703922.1:c.911-20_911-18delinsTTG ENSP00000515557.1:n.911-20_911-18delinsTTG
ENST00000703923.1:c.824-20_824-18delinsTTG ENSP00000515558.1:n.824-20_824-18delinsTTG
ENST00000703924.1:c.911-20_911-18delinsTTG ENSP00000515559.1:n.911-20_911-18delinsTTG
ENST00000703978.1:c.998-20_998-18delinsTTG ENSP00000515600.1:n.998-20_998-18delinsTTG
ENST00000703979.1:n.769-20_769-18delinsTTG
ENST00000703980.1:n.224-20_224-18delinsTTG
ENST00000703981.1:n.182-20_182-18delinsTTG
ENST00000703982.1:n.396_398delinsTTG
ENST00000262410.10:c.2174-20_2174-18delinsTTG MANE Select ENSP00000262410.6:n.2174-20_2174-18delinsTTG
ENST00000344290.10:c.1883-20_1883-18delinsTTG ENSP00000340820.6:n.1883-20_1883-18delinsTTG
ENST00000351559.10:c.998-20_998-18delinsTTG ENSP00000303214.7:n.998-20_998-18delinsTTG
ENST00000535772.6:c.818-20_818-18delinsTTG ENSP00000443028.2:n.818-20_818-18delinsTTG
ENST00000680542.1:c.911-20_911-18delinsTTG ENSP00000505258.1:n.911-20_911-18delinsTTG
ENST00000680674.1:c.947-20_947-18delinsTTG ENSP00000505478.1:n.947-20_947-18delinsTTG
ENST00000262410.9:c.1949-20_1949-18delinsTTG ENSP00000262410.5:n.1949-20_1949-18delinsTTG
ENST00000334239.12:c.731-20_731-18delinsTTG ENSP00000334886.8:n.731-20_731-18delinsTTG
ENST00000340799.9:c.911-20_911-18delinsTTG ENSP00000340438.5:n.911-20_911-18delinsTTG
ENST00000344290.9:c.2003-20_2003-18delinsTTG ENSP00000340820.5:n.2003-20_2003-18delinsTTG
ENST00000351559.9:c.998-20_998-18delinsTTG ENSP00000303214.7:n.998-20_998-18delinsTTG
ENST00000415613.6:c.2003-20_2003-18delinsTTG ENSP00000410838.2:n.2003-20_2003-18delinsTTG
ENST00000420682.6:c.911-20_911-18delinsTTG ENSP00000413056.2:n.911-20_911-18delinsTTG
ENST00000431008.7:c.905-20_905-18delinsTTG ENSP00000389250.3:n.905-20_905-18delinsTTG
ENST00000446361.7:c.824-20_824-18delinsTTG ENSP00000408975.3:n.824-20_824-18delinsTTG
ENST00000535772.5:c.905-20_905-18delinsTTG ENSP00000443028.1:n.905-20_905-18delinsTTG
ENST00000570299.5:n.777-20_777-18delinsTTG
ENST00000571987.5:c.1949-20_1949-18delinsTTG ENSP00000458742.1:n.1949-20_1949-18delinsTTG
ENST00000574436.5:c.998-20_998-18delinsTTG ENSP00000460965.1:n.998-20_998-18delinsTTG
ENST00000576518.1:n.6190-20_6190-18delinsTTG
NM_001123066.3:c.2003-20_2003-18delinsTTG NP_001116538.2:n.2003-20_2003-18delinsTTG
NM_001123067.3:c.911-20_911-18delinsTTG NP_001116539.1:n.911-20_911-18delinsTTG
NM_001203251.1:c.818-20_818-18delinsTTG NP_001190180.1:n.818-20_818-18delinsTTG
NM_001203252.1:c.905-20_905-18delinsTTG NP_001190181.1:n.905-20_905-18delinsTTG
NM_005910.5:c.998-20_998-18delinsTTG NP_005901.2:n.998-20_998-18delinsTTG
NM_016834.4:c.824-20_824-18delinsTTG NP_058518.1:n.824-20_824-18delinsTTG
NM_016835.4:c.1949-20_1949-18delinsTTG NP_058519.3:n.1949-20_1949-18delinsTTG
NM_016841.4:c.731-20_731-18delinsTTG NP_058525.1:n.731-20_731-18delinsTTG
XM_005257362.3:c.2261-20_2261-18delinsTTG XP_005257419.1:n.2261-20_2261-18delinsTTG
XM_005257364.3:c.2174-20_2174-18delinsTTG XP_005257421.1:n.2174-20_2174-18delinsTTG
XM_005257365.3:c.2168-20_2168-18delinsTTG XP_005257422.1:n.2168-20_2168-18delinsTTG
XM_005257366.2:c.2087-20_2087-18delinsTTG XP_005257423.1:n.2087-20_2087-18delinsTTG
XM_005257367.3:c.2063-20_2063-18delinsTTG XP_005257424.1:n.2063-20_2063-18delinsTTG
XM_005257368.3:c.1970-20_1970-18delinsTTG XP_005257425.1:n.1970-20_1970-18delinsTTG
XM_005257369.3:c.1196-20_1196-18delinsTTG XP_005257426.1:n.1196-20_1196-18delinsTTG
XM_005257370.3:c.1109-20_1109-18delinsTTG XP_005257427.1:n.1109-20_1109-18delinsTTG
XM_005257371.3:c.1022-20_1022-18delinsTTG XP_005257428.1:n.1022-20_1022-18delinsTTG
XM_005257362.4:c.2261-20_2261-18delinsTTG XP_005257419.1:n.2261-20_2261-18delinsTTG
XM_005257364.4:c.2174-20_2174-18delinsTTG XP_005257421.1:n.2174-20_2174-18delinsTTG
XM_005257365.4:c.2168-20_2168-18delinsTTG XP_005257422.1:n.2168-20_2168-18delinsTTG
XM_005257366.3:c.2087-20_2087-18delinsTTG XP_005257423.1:n.2087-20_2087-18delinsTTG
XM_005257367.4:c.2063-20_2063-18delinsTTG XP_005257424.1:n.2063-20_2063-18delinsTTG
XM_005257368.4:c.1970-20_1970-18delinsTTG XP_005257425.1:n.1970-20_1970-18delinsTTG
XM_005257369.4:c.1196-20_1196-18delinsTTG XP_005257426.1:n.1196-20_1196-18delinsTTG
XM_005257370.4:c.1109-20_1109-18delinsTTG XP_005257427.1:n.1109-20_1109-18delinsTTG
XM_005257371.4:c.1022-20_1022-18delinsTTG XP_005257428.1:n.1022-20_1022-18delinsTTG
NM_001203251.2:c.818-20_818-18delinsTTG NP_001190180.1:n.818-20_818-18delinsTTG
NM_001377265.1:c.2174-20_2174-18delinsTTG MANE Select NP_001364194.1:n.2174-20_2174-18delinsTTG
NM_001377266.1:c.1883-20_1883-18delinsTTG NP_001364195.1:n.1883-20_1883-18delinsTTG
NM_001377267.1:c.771+4320_771+4322delinsTTG NP_001364196.1:n.771+4320_771+4322delinsTTG
NM_001377268.1:c.731-20_731-18delinsTTG NP_001364197.1:n.731-20_731-18delinsTTG
NM_016834.5:c.824-20_824-18delinsTTG NP_058518.1:n.824-20_824-18delinsTTG
NM_016841.5:c.731-20_731-18delinsTTG NP_058525.1:n.731-20_731-18delinsTTG
NR_165166.1:n.829-20_829-18delinsTTG
NM_001123066.4:c.2003-20_2003-18delinsTTG NP_001116538.2:n.2003-20_2003-18delinsTTG
NM_001123067.4:c.911-20_911-18delinsTTG NP_001116539.1:n.911-20_911-18delinsTTG
NM_001203252.2:c.905-20_905-18delinsTTG NP_001190181.1:n.905-20_905-18delinsTTG
NM_005910.6:c.998-20_998-18delinsTTG NP_005901.2:n.998-20_998-18delinsTTG
NM_016835.5:c.1949-20_1949-18delinsTTG NP_058519.3:n.1949-20_1949-18delinsTTG