Canonical Allele Identifier: CA399984584
Gene: MAPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46024108C>G , CM000679.2:g.46024108C>G GRCh38
NC_000017.10:g.44101474C>G , CM000679.1:g.44101474C>G GRCh37
NC_000017.9:g.41457319C>G NCBI36
NG_007398.1:g.134696C>G
NG_007398.2:g.134646C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000420682.7:c.1176C>G ENSP00000413056.2:p.Asp392Glu
ENST00000703922.1:c.1176C>G ENSP00000515557.1:p.Asp392Glu
ENST00000703923.1:c.1089C>G ENSP00000515558.1:p.Asp363Glu
ENST00000703924.1:c.1176C>G ENSP00000515559.1:p.Asp392Glu
ENST00000703978.1:c.1263C>G ENSP00000515600.1:p.Asp421Glu
ENST00000703980.1:n.489C>G
ENST00000703981.1:n.447C>G
ENST00000703982.1:n.681C>G
ENST00000262410.10:c.2439C>G MANE Select ENSP00000262410.6:p.Asp813Glu
ENST00000344290.10:c.2148C>G ENSP00000340820.6:p.Asp716Glu
ENST00000351559.10:c.1263C>G ENSP00000303214.7:p.Asp421Glu
ENST00000535772.6:c.1083C>G ENSP00000443028.2:p.Asp361Glu
ENST00000680542.1:c.1176C>G ENSP00000505258.1:p.Asp392Glu
ENST00000680674.1:c.1212C>G ENSP00000505478.1:p.Asp404Glu
ENST00000262410.9:c.2214C>G ENSP00000262410.5:p.Asp738Glu
ENST00000334239.12:c.996C>G ENSP00000334886.8:p.Asp332Glu
ENST00000340799.9:c.1176C>G ENSP00000340438.5:p.Asp392Glu
ENST00000344290.9:c.2268C>G ENSP00000340820.5:p.Asp756Glu
ENST00000351559.9:c.1263C>G ENSP00000303214.7:p.Asp421Glu
ENST00000415613.6:c.2268C>G ENSP00000410838.2:p.Asp756Glu
ENST00000420682.6:c.1176C>G ENSP00000413056.2:p.Asp392Glu
ENST00000431008.7:c.1170C>G ENSP00000389250.3:p.Asp390Glu
ENST00000446361.7:c.1089C>G ENSP00000408975.3:p.Asp363Glu
ENST00000535772.5:c.1170C>G ENSP00000443028.1:p.Asp390Glu
ENST00000571987.5:c.2214C>G ENSP00000458742.1:p.Asp738Glu
ENST00000574436.5:c.1263C>G ENSP00000460965.1:p.Asp421Glu
ENST00000576518.1:n.6455C>G
NM_001123066.3:c.2268C>G NP_001116538.2:p.Asp756Glu
NM_001123067.3:c.1176C>G NP_001116539.1:p.Asp392Glu
NM_001203251.1:c.1083C>G NP_001190180.1:p.Asp361Glu
NM_001203252.1:c.1170C>G NP_001190181.1:p.Asp390Glu
NM_005910.5:c.1263C>G NP_005901.2:p.Asp421Glu
NM_016834.4:c.1089C>G NP_058518.1:p.Asp363Glu
NM_016835.4:c.2214C>G NP_058519.3:p.Asp738Glu
NM_016841.4:c.996C>G NP_058525.1:p.Asp332Glu
XM_005257362.3:c.2526C>G XP_005257419.1:p.Asp842Glu
XM_005257364.3:c.2439C>G XP_005257421.1:p.Asp813Glu
XM_005257365.3:c.2433C>G XP_005257422.1:p.Asp811Glu
XM_005257366.2:c.2352C>G XP_005257423.1:p.Asp784Glu
XM_005257367.3:c.2328C>G XP_005257424.1:p.Asp776Glu
XM_005257368.3:c.2235C>G XP_005257425.1:p.Asp745Glu
XM_005257369.3:c.1461C>G XP_005257426.1:p.Asp487Glu
XM_005257370.3:c.1374C>G XP_005257427.1:p.Asp458Glu
XM_005257371.3:c.1287C>G XP_005257428.1:p.Asp429Glu
XM_005257362.4:c.2526C>G XP_005257419.1:p.Asp842Glu
XM_005257364.4:c.2439C>G XP_005257421.1:p.Asp813Glu
XM_005257365.4:c.2433C>G XP_005257422.1:p.Asp811Glu
XM_005257366.3:c.2352C>G XP_005257423.1:p.Asp784Glu
XM_005257367.4:c.2328C>G XP_005257424.1:p.Asp776Glu
XM_005257368.4:c.2235C>G XP_005257425.1:p.Asp745Glu
XM_005257369.4:c.1461C>G XP_005257426.1:p.Asp487Glu
XM_005257370.4:c.1374C>G XP_005257427.1:p.Asp458Glu
XM_005257371.4:c.1287C>G XP_005257428.1:p.Asp429Glu
NM_001203251.2:c.1083C>G NP_001190180.1:p.Asp361Glu
NM_001377265.1:c.2439C>G MANE Select NP_001364194.1:p.Asp813Glu
NM_001377266.1:c.2148C>G NP_001364195.1:p.Asp716Glu
NM_001377267.1:c.772-1009C>G NP_001364196.1:n.772-1009C>G
NM_001377268.1:c.996C>G NP_001364197.1:p.Asp332Glu
NM_016834.5:c.1089C>G NP_058518.1:p.Asp363Glu
NM_016841.5:c.996C>G NP_058525.1:p.Asp332Glu
NR_165166.1:n.1094C>G
NM_001123066.4:c.2268C>G NP_001116538.2:p.Asp756Glu
NM_001123067.4:c.1176C>G NP_001116539.1:p.Asp392Glu
NM_001203252.2:c.1170C>G NP_001190181.1:p.Asp390Glu
NM_005910.6:c.1263C>G NP_005901.2:p.Asp421Glu
NM_016835.5:c.2214C>G NP_058519.3:p.Asp738Glu