Canonical Allele Identifier: CA1616765609

Gene: SLC17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812872G= , CM000668.2:g.25812872G=	GRCh38
NC_000006.11:g.25813100G= , CM000668.1:g.25813100G=	GRCh37
NC_000006.10:g.25921079G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.856C= MANE Select	ENSP00000244527.4:p.Pro286=
ENST00000244527.8:c.856C=	ENSP00000244527.4:p.Pro286=
ENST00000377886.6:c.*107C=	ENSP00000367118.2:n.*107C=
ENST00000468082.1:c.735+223C=	ENSP00000420546.1:n.735+223C=
ENST00000476801.5:c.856C=	ENSP00000420614.1:p.Pro286=
NM_005074.3:c.856C=	NP_005065.2:p.Pro286=
XM_011514818.1:c.856C=	XP_011513120.1:p.Pro286=
XM_011514819.1:c.769C=	XP_011513121.1:p.Pro257=
XM_011514820.1:c.735+223C=	XP_011513122.1:n.735+223C=
XM_011514821.1:c.643C=	XP_011513123.1:p.Pro215=
XM_011514818.2:c.1006C=	XP_011513120.2:p.Pro336=
XM_011514819.2:c.919C=	XP_011513121.2:p.Pro307=
XM_011514820.2:c.885+223C=	XP_011513122.2:n.885+223C=
XM_011514821.2:c.643C=	XP_011513123.1:p.Pro215=
XM_017011199.1:c.1006C=	XP_016866688.1:p.Pro336=
XM_017011200.1:c.1006C=	XP_016866689.1:p.Pro336=
XM_017011201.2:c.1006C=	XP_016866690.1:p.Pro336=
XM_017011202.1:c.922C=	XP_016866691.1:p.Pro308=
NM_005074.5:c.856C= MANE Select	NP_005065.2:p.Pro286=