Canonical Allele Identifier: CA399983511
Gene: MAPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46014286C>A , CM000679.2:g.46014286C>A GRCh38
NC_000017.10:g.44091652C>A , CM000679.1:g.44091652C>A GRCh37
NC_000017.9:g.41447489C>A NCBI36
NG_007398.1:g.124866C>A
NG_007398.2:g.124824C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420682.7:c.872C>A ENSP00000413056.2:p.Ser291Tyr
ENST00000703922.1:c.872C>A ENSP00000515557.1:p.Ser291Tyr
ENST00000703923.1:c.785C>A ENSP00000515558.1:p.Ser262Tyr
ENST00000703924.1:c.872C>A ENSP00000515559.1:p.Ser291Tyr
ENST00000703978.1:c.959C>A ENSP00000515600.1:p.Ser320Tyr
ENST00000703979.1:n.730C>A
ENST00000703980.1:n.185C>A
ENST00000703981.1:n.128C>A
ENST00000262410.10:c.2135C>A MANE Select ENSP00000262410.6:p.Ser712Tyr
ENST00000344290.10:c.1844C>A ENSP00000340820.6:p.Ser615Tyr
ENST00000351559.10:c.959C>A ENSP00000303214.7:p.Ser320Tyr
ENST00000535772.6:c.779C>A ENSP00000443028.2:p.Ser260Tyr
ENST00000680542.1:c.872C>A ENSP00000505258.1:p.Ser291Tyr
ENST00000680674.1:c.785C>A ENSP00000505478.1:p.Ser262Tyr
ENST00000262410.9:c.1910C>A ENSP00000262410.5:p.Ser637Tyr
ENST00000334239.12:c.692C>A ENSP00000334886.8:p.Ser231Tyr
ENST00000340799.9:c.872C>A ENSP00000340438.5:p.Ser291Tyr
ENST00000344290.9:c.1964C>A ENSP00000340820.5:p.Ser655Tyr
ENST00000351559.9:c.959C>A ENSP00000303214.7:p.Ser320Tyr
ENST00000415613.6:c.1964C>A ENSP00000410838.2:p.Ser655Tyr
ENST00000420682.6:c.872C>A ENSP00000413056.2:p.Ser291Tyr
ENST00000431008.7:c.866C>A ENSP00000389250.3:p.Ser289Tyr
ENST00000446361.7:c.785C>A ENSP00000408975.3:p.Ser262Tyr
ENST00000535772.5:c.866C>A ENSP00000443028.1:p.Ser289Tyr
ENST00000570299.5:n.777-4332C>A
ENST00000571987.5:c.1910C>A ENSP00000458742.1:p.Ser637Tyr
ENST00000574436.5:c.959C>A ENSP00000460965.1:p.Ser320Tyr
ENST00000576518.1:n.6151C>A
NM_001123066.3:c.1964C>A NP_001116538.2:p.Ser655Tyr
NM_001123067.3:c.872C>A NP_001116539.1:p.Ser291Tyr
NM_001203251.1:c.779C>A NP_001190180.1:p.Ser260Tyr
NM_001203252.1:c.866C>A NP_001190181.1:p.Ser289Tyr
NM_005910.5:c.959C>A NP_005901.2:p.Ser320Tyr
NM_016834.4:c.785C>A NP_058518.1:p.Ser262Tyr
NM_016835.4:c.1910C>A NP_058519.3:p.Ser637Tyr
NM_016841.4:c.692C>A NP_058525.1:p.Ser231Tyr
XM_005257362.3:c.2222C>A XP_005257419.1:p.Ser741Tyr
XM_005257364.3:c.2135C>A XP_005257421.1:p.Ser712Tyr
XM_005257365.3:c.2129C>A XP_005257422.1:p.Ser710Tyr
XM_005257366.2:c.2048C>A XP_005257423.1:p.Ser683Tyr
XM_005257367.3:c.2024C>A XP_005257424.1:p.Ser675Tyr
XM_005257368.3:c.1931C>A XP_005257425.1:p.Ser644Tyr
XM_005257369.3:c.1157C>A XP_005257426.1:p.Ser386Tyr
XM_005257370.3:c.1070C>A XP_005257427.1:p.Ser357Tyr
XM_005257371.3:c.983C>A XP_005257428.1:p.Ser328Tyr
XM_005257362.4:c.2222C>A XP_005257419.1:p.Ser741Tyr
XM_005257364.4:c.2135C>A XP_005257421.1:p.Ser712Tyr
XM_005257365.4:c.2129C>A XP_005257422.1:p.Ser710Tyr
XM_005257366.3:c.2048C>A XP_005257423.1:p.Ser683Tyr
XM_005257367.4:c.2024C>A XP_005257424.1:p.Ser675Tyr
XM_005257368.4:c.1931C>A XP_005257425.1:p.Ser644Tyr
XM_005257369.4:c.1157C>A XP_005257426.1:p.Ser386Tyr
XM_005257370.4:c.1070C>A XP_005257427.1:p.Ser357Tyr
XM_005257371.4:c.983C>A XP_005257428.1:p.Ser328Tyr
NM_001203251.2:c.779C>A NP_001190180.1:p.Ser260Tyr
NM_001377265.1:c.2135C>A MANE Select NP_001364194.1:p.Ser712Tyr
NM_001377266.1:c.1844C>A NP_001364195.1:p.Ser615Tyr
NM_001377267.1:c.771+8C>A NP_001364196.1:n.771+8C>A
NM_001377268.1:c.692C>A NP_001364197.1:p.Ser231Tyr
NM_016834.5:c.785C>A NP_058518.1:p.Ser262Tyr
NM_016841.5:c.692C>A NP_058525.1:p.Ser231Tyr
NR_165166.1:n.790C>A
NM_001123066.4:c.1964C>A NP_001116538.2:p.Ser655Tyr
NM_001123067.4:c.872C>A NP_001116539.1:p.Ser291Tyr
NM_001203252.2:c.866C>A NP_001190181.1:p.Ser289Tyr
NM_005910.6:c.959C>A NP_005901.2:p.Ser320Tyr
NM_016835.5:c.1910C>A NP_058519.3:p.Ser637Tyr