Canonical Allele Identifier: CA1616765653

Gene: SLC17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812979C= , CM000668.2:g.25812979C=	GRCh38
NC_000006.11:g.25813207C= , CM000668.1:g.25813207C=	GRCh37
NC_000006.10:g.25921186C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.749G= MANE Select	ENSP00000244527.4:p.Arg250=
ENST00000244527.8:c.749G=	ENSP00000244527.4:p.Arg250=
ENST00000377886.6:c.630G=	ENSP00000367118.2:p.Ter210=
ENST00000468082.1:c.735+116G=	ENSP00000420546.1:n.735+116G=
ENST00000476801.5:c.749G=	ENSP00000420614.1:p.Arg250=
NM_005074.3:c.749G=	NP_005065.2:p.Arg250=
XM_011514818.1:c.749G=	XP_011513120.1:p.Arg250=
XM_011514819.1:c.662G=	XP_011513121.1:p.Arg221=
XM_011514820.1:c.735+116G=	XP_011513122.1:n.735+116G=
XM_011514821.1:c.536G=	XP_011513123.1:p.Arg179=
XM_011514818.2:c.899G=	XP_011513120.2:p.Arg300=
XM_011514819.2:c.812G=	XP_011513121.2:p.Arg271=
XM_011514820.2:c.885+116G=	XP_011513122.2:n.885+116G=
XM_011514821.2:c.536G=	XP_011513123.1:p.Arg179=
XM_017011199.1:c.899G=	XP_016866688.1:p.Arg300=
XM_017011200.1:c.899G=	XP_016866689.1:p.Arg300=
XM_017011201.2:c.899G=	XP_016866690.1:p.Arg300=
XM_017011202.1:c.815G=	XP_016866691.1:p.Arg272=
NM_005074.5:c.749G= MANE Select	NP_005065.2:p.Arg250=