Canonical Allele Identifier: CA500371187

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44091653C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46014287C>A , CM000679.2:g.46014287C>A	GRCh38
NC_000017.10:g.44091653C>A , CM000679.1:g.44091653C>A	GRCh37
NC_000017.9:g.41447490C>A	NCBI36
NG_007398.1:g.124867C>A
NG_007398.2:g.124825C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.873C>A	ENSP00000413056.2:p.Ser291=
ENST00000703922.1:c.873C>A	ENSP00000515557.1:p.Ser291=
ENST00000703923.1:c.786C>A	ENSP00000515558.1:p.Ser262=
ENST00000703924.1:c.873C>A	ENSP00000515559.1:p.Ser291=
ENST00000703978.1:c.960C>A	ENSP00000515600.1:p.Ser320=
ENST00000703979.1:n.731C>A
ENST00000703980.1:n.186C>A
ENST00000703981.1:n.129C>A
ENST00000262410.10:c.2136C>A MANE Select	ENSP00000262410.6:p.Ser712=
ENST00000344290.10:c.1845C>A	ENSP00000340820.6:p.Ser615=
ENST00000351559.10:c.960C>A	ENSP00000303214.7:p.Ser320=
ENST00000535772.6:c.780C>A	ENSP00000443028.2:p.Ser260=
ENST00000680542.1:c.873C>A	ENSP00000505258.1:p.Ser291=
ENST00000680674.1:c.786C>A	ENSP00000505478.1:p.Ser262=
ENST00000262410.9:c.1911C>A	ENSP00000262410.5:p.Ser637=
ENST00000334239.12:c.693C>A	ENSP00000334886.8:p.Ser231=
ENST00000340799.9:c.873C>A	ENSP00000340438.5:p.Ser291=
ENST00000344290.9:c.1965C>A	ENSP00000340820.5:p.Ser655=
ENST00000351559.9:c.960C>A	ENSP00000303214.7:p.Ser320=
ENST00000415613.6:c.1965C>A	ENSP00000410838.2:p.Ser655=
ENST00000420682.6:c.873C>A	ENSP00000413056.2:p.Ser291=
ENST00000431008.7:c.867C>A	ENSP00000389250.3:p.Ser289=
ENST00000446361.7:c.786C>A	ENSP00000408975.3:p.Ser262=
ENST00000535772.5:c.867C>A	ENSP00000443028.1:p.Ser289=
ENST00000570299.5:n.777-4331C>A
ENST00000571987.5:c.1911C>A	ENSP00000458742.1:p.Ser637=
ENST00000574436.5:c.960C>A	ENSP00000460965.1:p.Ser320=
ENST00000576518.1:n.6152C>A
NM_001123066.3:c.1965C>A	NP_001116538.2:p.Ser655=
NM_001123067.3:c.873C>A	NP_001116539.1:p.Ser291=
NM_001203251.1:c.780C>A	NP_001190180.1:p.Ser260=
NM_001203252.1:c.867C>A	NP_001190181.1:p.Ser289=
NM_005910.5:c.960C>A	NP_005901.2:p.Ser320=
NM_016834.4:c.786C>A	NP_058518.1:p.Ser262=
NM_016835.4:c.1911C>A	NP_058519.3:p.Ser637=
NM_016841.4:c.693C>A	NP_058525.1:p.Ser231=
XM_005257362.3:c.2223C>A	XP_005257419.1:p.Ser741=
XM_005257364.3:c.2136C>A	XP_005257421.1:p.Ser712=
XM_005257365.3:c.2130C>A	XP_005257422.1:p.Ser710=
XM_005257366.2:c.2049C>A	XP_005257423.1:p.Ser683=
XM_005257367.3:c.2025C>A	XP_005257424.1:p.Ser675=
XM_005257368.3:c.1932C>A	XP_005257425.1:p.Ser644=
XM_005257369.3:c.1158C>A	XP_005257426.1:p.Ser386=
XM_005257370.3:c.1071C>A	XP_005257427.1:p.Ser357=
XM_005257371.3:c.984C>A	XP_005257428.1:p.Ser328=
XM_005257362.4:c.2223C>A	XP_005257419.1:p.Ser741=
XM_005257364.4:c.2136C>A	XP_005257421.1:p.Ser712=
XM_005257365.4:c.2130C>A	XP_005257422.1:p.Ser710=
XM_005257366.3:c.2049C>A	XP_005257423.1:p.Ser683=
XM_005257367.4:c.2025C>A	XP_005257424.1:p.Ser675=
XM_005257368.4:c.1932C>A	XP_005257425.1:p.Ser644=
XM_005257369.4:c.1158C>A	XP_005257426.1:p.Ser386=
XM_005257370.4:c.1071C>A	XP_005257427.1:p.Ser357=
XM_005257371.4:c.984C>A	XP_005257428.1:p.Ser328=
NM_001203251.2:c.780C>A	NP_001190180.1:p.Ser260=
NM_001377265.1:c.2136C>A MANE Select	NP_001364194.1:p.Ser712=
NM_001377266.1:c.1845C>A	NP_001364195.1:p.Ser615=
NM_001377267.1:c.771+9C>A	NP_001364196.1:n.771+9C>A
NM_001377268.1:c.693C>A	NP_001364197.1:p.Ser231=
NM_016834.5:c.786C>A	NP_058518.1:p.Ser262=
NM_016841.5:c.693C>A	NP_058525.1:p.Ser231=
NR_165166.1:n.791C>A
NM_001123066.4:c.1965C>A	NP_001116538.2:p.Ser655=
NM_001123067.4:c.873C>A	NP_001116539.1:p.Ser291=
NM_001203252.2:c.867C>A	NP_001190181.1:p.Ser289=
NM_005910.6:c.960C>A	NP_005901.2:p.Ser320=
NM_016835.5:c.1911C>A	NP_058519.3:p.Ser637=