Canonical Allele Identifier: CA399983639

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44095996T>G (hg19) ; chr17:g.46018630T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46018630T>G , CM000679.2:g.46018630T>G	GRCh38
NC_000017.10:g.44095996T>G , CM000679.1:g.44095996T>G	GRCh37
NC_000017.9:g.41451843T>G	NCBI36
NG_007398.1:g.129220T>G
NG_007398.2:g.129168T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.923T>G	ENSP00000413056.2:p.Val308Gly
ENST00000703922.1:c.923T>G	ENSP00000515557.1:p.Val308Gly
ENST00000703923.1:c.836T>G	ENSP00000515558.1:p.Val279Gly
ENST00000703924.1:c.923T>G	ENSP00000515559.1:p.Val308Gly
ENST00000703978.1:c.1010T>G	ENSP00000515600.1:p.Val337Gly
ENST00000703979.1:n.781T>G
ENST00000703980.1:n.236T>G
ENST00000703981.1:n.194T>G
ENST00000703982.1:n.428T>G
ENST00000262410.10:c.2186T>G MANE Select	ENSP00000262410.6:p.Val729Gly
ENST00000344290.10:c.1895T>G	ENSP00000340820.6:p.Val632Gly
ENST00000351559.10:c.1010T>G	ENSP00000303214.7:p.Val337Gly
ENST00000535772.6:c.830T>G	ENSP00000443028.2:p.Val277Gly
ENST00000680542.1:c.923T>G	ENSP00000505258.1:p.Val308Gly
ENST00000680674.1:c.959T>G	ENSP00000505478.1:p.Val320Gly
ENST00000262410.9:c.1961T>G	ENSP00000262410.5:p.Val654Gly
ENST00000334239.12:c.743T>G	ENSP00000334886.8:p.Val248Gly
ENST00000340799.9:c.923T>G	ENSP00000340438.5:p.Val308Gly
ENST00000344290.9:c.2015T>G	ENSP00000340820.5:p.Val672Gly
ENST00000351559.9:c.1010T>G	ENSP00000303214.7:p.Val337Gly
ENST00000415613.6:c.2015T>G	ENSP00000410838.2:p.Val672Gly
ENST00000420682.6:c.923T>G	ENSP00000413056.2:p.Val308Gly
ENST00000431008.7:c.917T>G	ENSP00000389250.3:p.Val306Gly
ENST00000446361.7:c.836T>G	ENSP00000408975.3:p.Val279Gly
ENST00000535772.5:c.917T>G	ENSP00000443028.1:p.Val306Gly
ENST00000570299.5:n.789T>G
ENST00000571987.5:c.1961T>G	ENSP00000458742.1:p.Val654Gly
ENST00000574436.5:c.1010T>G	ENSP00000460965.1:p.Val337Gly
ENST00000576518.1:n.6202T>G
NM_001123066.3:c.2015T>G	NP_001116538.2:p.Val672Gly
NM_001123067.3:c.923T>G	NP_001116539.1:p.Val308Gly
NM_001203251.1:c.830T>G	NP_001190180.1:p.Val277Gly
NM_001203252.1:c.917T>G	NP_001190181.1:p.Val306Gly
NM_005910.5:c.1010T>G	NP_005901.2:p.Val337Gly
NM_016834.4:c.836T>G	NP_058518.1:p.Val279Gly
NM_016835.4:c.1961T>G	NP_058519.3:p.Val654Gly
NM_016841.4:c.743T>G	NP_058525.1:p.Val248Gly
XM_005257362.3:c.2273T>G	XP_005257419.1:p.Val758Gly
XM_005257364.3:c.2186T>G	XP_005257421.1:p.Val729Gly
XM_005257365.3:c.2180T>G	XP_005257422.1:p.Val727Gly
XM_005257366.2:c.2099T>G	XP_005257423.1:p.Val700Gly
XM_005257367.3:c.2075T>G	XP_005257424.1:p.Val692Gly
XM_005257368.3:c.1982T>G	XP_005257425.1:p.Val661Gly
XM_005257369.3:c.1208T>G	XP_005257426.1:p.Val403Gly
XM_005257370.3:c.1121T>G	XP_005257427.1:p.Val374Gly
XM_005257371.3:c.1034T>G	XP_005257428.1:p.Val345Gly
XM_005257362.4:c.2273T>G	XP_005257419.1:p.Val758Gly
XM_005257364.4:c.2186T>G	XP_005257421.1:p.Val729Gly
XM_005257365.4:c.2180T>G	XP_005257422.1:p.Val727Gly
XM_005257366.3:c.2099T>G	XP_005257423.1:p.Val700Gly
XM_005257367.4:c.2075T>G	XP_005257424.1:p.Val692Gly
XM_005257368.4:c.1982T>G	XP_005257425.1:p.Val661Gly
XM_005257369.4:c.1208T>G	XP_005257426.1:p.Val403Gly
XM_005257370.4:c.1121T>G	XP_005257427.1:p.Val374Gly
XM_005257371.4:c.1034T>G	XP_005257428.1:p.Val345Gly
NM_001203251.2:c.830T>G	NP_001190180.1:p.Val277Gly
NM_001377265.1:c.2186T>G MANE Select	NP_001364194.1:p.Val729Gly
NM_001377266.1:c.1895T>G	NP_001364195.1:p.Val632Gly
NM_001377267.1:c.771+4352T>G	NP_001364196.1:n.771+4352T>G
NM_001377268.1:c.743T>G	NP_001364197.1:p.Val248Gly
NM_016834.5:c.836T>G	NP_058518.1:p.Val279Gly
NM_016841.5:c.743T>G	NP_058525.1:p.Val248Gly
NR_165166.1:n.841T>G
NM_001123066.4:c.2015T>G	NP_001116538.2:p.Val672Gly
NM_001123067.4:c.923T>G	NP_001116539.1:p.Val308Gly
NM_001203252.2:c.917T>G	NP_001190181.1:p.Val306Gly
NM_005910.6:c.1010T>G	NP_005901.2:p.Val337Gly
NM_016835.5:c.1961T>G	NP_058519.3:p.Val654Gly