Canonical Allele Identifier: CA399983528
Gene: MAPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46014293T>A , CM000679.2:g.46014293T>A GRCh38
NC_000017.10:g.44091659T>A , CM000679.1:g.44091659T>A GRCh37
NC_000017.9:g.41447496T>A NCBI36
NG_007398.1:g.124873T>A
NG_007398.2:g.124831T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420682.7:c.879T>A ENSP00000413056.2:p.Cys293Ter
ENST00000703922.1:c.879T>A ENSP00000515557.1:p.Cys293Ter
ENST00000703923.1:c.792T>A ENSP00000515558.1:p.Cys264Ter
ENST00000703924.1:c.879T>A ENSP00000515559.1:p.Cys293Ter
ENST00000703978.1:c.966T>A ENSP00000515600.1:p.Cys322Ter
ENST00000703979.1:n.737T>A
ENST00000703980.1:n.192T>A
ENST00000703981.1:n.135T>A
ENST00000262410.10:c.2142T>A MANE Select ENSP00000262410.6:p.Cys714Ter
ENST00000344290.10:c.1851T>A ENSP00000340820.6:p.Cys617Ter
ENST00000351559.10:c.966T>A ENSP00000303214.7:p.Cys322Ter
ENST00000535772.6:c.786T>A ENSP00000443028.2:p.Cys262Ter
ENST00000680542.1:c.879T>A ENSP00000505258.1:p.Cys293Ter
ENST00000680674.1:c.792T>A ENSP00000505478.1:p.Cys264Ter
ENST00000262410.9:c.1917T>A ENSP00000262410.5:p.Cys639Ter
ENST00000334239.12:c.699T>A ENSP00000334886.8:p.Cys233Ter
ENST00000340799.9:c.879T>A ENSP00000340438.5:p.Cys293Ter
ENST00000344290.9:c.1971T>A ENSP00000340820.5:p.Cys657Ter
ENST00000351559.9:c.966T>A ENSP00000303214.7:p.Cys322Ter
ENST00000415613.6:c.1971T>A ENSP00000410838.2:p.Cys657Ter
ENST00000420682.6:c.879T>A ENSP00000413056.2:p.Cys293Ter
ENST00000431008.7:c.873T>A ENSP00000389250.3:p.Cys291Ter
ENST00000446361.7:c.792T>A ENSP00000408975.3:p.Cys264Ter
ENST00000535772.5:c.873T>A ENSP00000443028.1:p.Cys291Ter
ENST00000570299.5:n.777-4325T>A
ENST00000571987.5:c.1917T>A ENSP00000458742.1:p.Cys639Ter
ENST00000574436.5:c.966T>A ENSP00000460965.1:p.Cys322Ter
ENST00000576518.1:n.6158T>A
NM_001123066.3:c.1971T>A NP_001116538.2:p.Cys657Ter
NM_001123067.3:c.879T>A NP_001116539.1:p.Cys293Ter
NM_001203251.1:c.786T>A NP_001190180.1:p.Cys262Ter
NM_001203252.1:c.873T>A NP_001190181.1:p.Cys291Ter
NM_005910.5:c.966T>A NP_005901.2:p.Cys322Ter
NM_016834.4:c.792T>A NP_058518.1:p.Cys264Ter
NM_016835.4:c.1917T>A NP_058519.3:p.Cys639Ter
NM_016841.4:c.699T>A NP_058525.1:p.Cys233Ter
XM_005257362.3:c.2229T>A XP_005257419.1:p.Cys743Ter
XM_005257364.3:c.2142T>A XP_005257421.1:p.Cys714Ter
XM_005257365.3:c.2136T>A XP_005257422.1:p.Cys712Ter
XM_005257366.2:c.2055T>A XP_005257423.1:p.Cys685Ter
XM_005257367.3:c.2031T>A XP_005257424.1:p.Cys677Ter
XM_005257368.3:c.1938T>A XP_005257425.1:p.Cys646Ter
XM_005257369.3:c.1164T>A XP_005257426.1:p.Cys388Ter
XM_005257370.3:c.1077T>A XP_005257427.1:p.Cys359Ter
XM_005257371.3:c.990T>A XP_005257428.1:p.Cys330Ter
XM_005257362.4:c.2229T>A XP_005257419.1:p.Cys743Ter
XM_005257364.4:c.2142T>A XP_005257421.1:p.Cys714Ter
XM_005257365.4:c.2136T>A XP_005257422.1:p.Cys712Ter
XM_005257366.3:c.2055T>A XP_005257423.1:p.Cys685Ter
XM_005257367.4:c.2031T>A XP_005257424.1:p.Cys677Ter
XM_005257368.4:c.1938T>A XP_005257425.1:p.Cys646Ter
XM_005257369.4:c.1164T>A XP_005257426.1:p.Cys388Ter
XM_005257370.4:c.1077T>A XP_005257427.1:p.Cys359Ter
XM_005257371.4:c.990T>A XP_005257428.1:p.Cys330Ter
NM_001203251.2:c.786T>A NP_001190180.1:p.Cys262Ter
NM_001377265.1:c.2142T>A MANE Select NP_001364194.1:p.Cys714Ter
NM_001377266.1:c.1851T>A NP_001364195.1:p.Cys617Ter
NM_001377267.1:c.771+15T>A NP_001364196.1:n.771+15T>A
NM_001377268.1:c.699T>A NP_001364197.1:p.Cys233Ter
NM_016834.5:c.792T>A NP_058518.1:p.Cys264Ter
NM_016841.5:c.699T>A NP_058525.1:p.Cys233Ter
NR_165166.1:n.797T>A
NM_001123066.4:c.1971T>A NP_001116538.2:p.Cys657Ter
NM_001123067.4:c.879T>A NP_001116539.1:p.Cys293Ter
NM_001203252.2:c.873T>A NP_001190181.1:p.Cys291Ter
NM_005910.6:c.966T>A NP_005901.2:p.Cys322Ter
NM_016835.5:c.1917T>A NP_058519.3:p.Cys639Ter