Canonical Allele Identifier: CA2262102723
Gene: MAPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46014296C= , CM000679.2:g.46014296C= GRCh38
NC_000017.10:g.44091662C= , CM000679.1:g.44091662C= GRCh37
NC_000017.9:g.41447499C= NCBI36
NG_007398.1:g.124876C=
NG_007398.2:g.124834C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420682.7:c.882C= ENSP00000413056.2:p.Gly294=
ENST00000703922.1:c.882C= ENSP00000515557.1:p.Gly294=
ENST00000703923.1:c.795C= ENSP00000515558.1:p.Gly265=
ENST00000703924.1:c.882C= ENSP00000515559.1:p.Gly294=
ENST00000703978.1:c.969C= ENSP00000515600.1:p.Gly323=
ENST00000703979.1:n.740C=
ENST00000703980.1:n.195C=
ENST00000703981.1:n.138C=
ENST00000262410.10:c.2145C= MANE Select ENSP00000262410.6:p.Gly715=
ENST00000344290.10:c.1854C= ENSP00000340820.6:p.Gly618=
ENST00000351559.10:c.969C= ENSP00000303214.7:p.Gly323=
ENST00000535772.6:c.789C= ENSP00000443028.2:p.Gly263=
ENST00000680542.1:c.882C= ENSP00000505258.1:p.Gly294=
ENST00000680674.1:c.795C= ENSP00000505478.1:p.Gly265=
ENST00000262410.9:c.1920C= ENSP00000262410.5:p.Gly640=
ENST00000334239.12:c.702C= ENSP00000334886.8:p.Gly234=
ENST00000340799.9:c.882C= ENSP00000340438.5:p.Gly294=
ENST00000344290.9:c.1974C= ENSP00000340820.5:p.Gly658=
ENST00000351559.9:c.969C= ENSP00000303214.7:p.Gly323=
ENST00000415613.6:c.1974C= ENSP00000410838.2:p.Gly658=
ENST00000420682.6:c.882C= ENSP00000413056.2:p.Gly294=
ENST00000431008.7:c.876C= ENSP00000389250.3:p.Gly292=
ENST00000446361.7:c.795C= ENSP00000408975.3:p.Gly265=
ENST00000535772.5:c.876C= ENSP00000443028.1:p.Gly292=
ENST00000570299.5:n.777-4322C=
ENST00000571987.5:c.1920C= ENSP00000458742.1:p.Gly640=
ENST00000574436.5:c.969C= ENSP00000460965.1:p.Gly323=
ENST00000576518.1:n.6161C=
NM_001123066.3:c.1974C= NP_001116538.2:p.Gly658=
NM_001123067.3:c.882C= NP_001116539.1:p.Gly294=
NM_001203251.1:c.789C= NP_001190180.1:p.Gly263=
NM_001203252.1:c.876C= NP_001190181.1:p.Gly292=
NM_005910.5:c.969C= NP_005901.2:p.Gly323=
NM_016834.4:c.795C= NP_058518.1:p.Gly265=
NM_016835.4:c.1920C= NP_058519.3:p.Gly640=
NM_016841.4:c.702C= NP_058525.1:p.Gly234=
XM_005257362.3:c.2232C= XP_005257419.1:p.Gly744=
XM_005257364.3:c.2145C= XP_005257421.1:p.Gly715=
XM_005257365.3:c.2139C= XP_005257422.1:p.Gly713=
XM_005257366.2:c.2058C= XP_005257423.1:p.Gly686=
XM_005257367.3:c.2034C= XP_005257424.1:p.Gly678=
XM_005257368.3:c.1941C= XP_005257425.1:p.Gly647=
XM_005257369.3:c.1167C= XP_005257426.1:p.Gly389=
XM_005257370.3:c.1080C= XP_005257427.1:p.Gly360=
XM_005257371.3:c.993C= XP_005257428.1:p.Gly331=
XM_005257362.4:c.2232C= XP_005257419.1:p.Gly744=
XM_005257364.4:c.2145C= XP_005257421.1:p.Gly715=
XM_005257365.4:c.2139C= XP_005257422.1:p.Gly713=
XM_005257366.3:c.2058C= XP_005257423.1:p.Gly686=
XM_005257367.4:c.2034C= XP_005257424.1:p.Gly678=
XM_005257368.4:c.1941C= XP_005257425.1:p.Gly647=
XM_005257369.4:c.1167C= XP_005257426.1:p.Gly389=
XM_005257370.4:c.1080C= XP_005257427.1:p.Gly360=
XM_005257371.4:c.993C= XP_005257428.1:p.Gly331=
NM_001203251.2:c.789C= NP_001190180.1:p.Gly263=
NM_001377265.1:c.2145C= MANE Select NP_001364194.1:p.Gly715=
NM_001377266.1:c.1854C= NP_001364195.1:p.Gly618=
NM_001377267.1:c.771+18C= NP_001364196.1:n.771+18C=
NM_001377268.1:c.702C= NP_001364197.1:p.Gly234=
NM_016834.5:c.795C= NP_058518.1:p.Gly265=
NM_016841.5:c.702C= NP_058525.1:p.Gly234=
NR_165166.1:n.800C=
NM_001123066.4:c.1974C= NP_001116538.2:p.Gly658=
NM_001123067.4:c.882C= NP_001116539.1:p.Gly294=
NM_001203252.2:c.876C= NP_001190181.1:p.Gly292=
NM_005910.6:c.969C= NP_005901.2:p.Gly323=
NM_016835.5:c.1920C= NP_058519.3:p.Gly640=