Canonical Allele Identifier: CA1616765634

Gene: SLC17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812932C= , CM000668.2:g.25812932C=	GRCh38
NC_000006.11:g.25813160C= , CM000668.1:g.25813160C=	GRCh37
NC_000006.10:g.25921139C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244527.10:c.796G= MANE Select	ENSP00000244527.4:p.Ala266=
ENST00000244527.8:c.796G=	ENSP00000244527.4:p.Ala266=
ENST00000377886.6:c.*47G=	ENSP00000367118.2:n.*47G=
ENST00000468082.1:c.735+163G=	ENSP00000420546.1:n.735+163G=
ENST00000476801.5:c.796G=	ENSP00000420614.1:p.Ala266=
NM_005074.3:c.796G=	NP_005065.2:p.Ala266=
XM_011514818.1:c.796G=	XP_011513120.1:p.Ala266=
XM_011514819.1:c.709G=	XP_011513121.1:p.Ala237=
XM_011514820.1:c.735+163G=	XP_011513122.1:n.735+163G=
XM_011514821.1:c.583G=	XP_011513123.1:p.Ala195=
XM_011514818.2:c.946G=	XP_011513120.2:p.Ala316=
XM_011514819.2:c.859G=	XP_011513121.2:p.Ala287=
XM_011514820.2:c.885+163G=	XP_011513122.2:n.885+163G=
XM_011514821.2:c.583G=	XP_011513123.1:p.Ala195=
XM_017011199.1:c.946G=	XP_016866688.1:p.Ala316=
XM_017011200.1:c.946G=	XP_016866689.1:p.Ala316=
XM_017011201.2:c.946G=	XP_016866690.1:p.Ala316=
XM_017011202.1:c.862G=	XP_016866691.1:p.Ala288=
NM_005074.5:c.796G= MANE Select	NP_005065.2:p.Ala266=