Canonical Allele Identifier: CA1616810466

Gene: SLC17A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25918539C= , CM000668.2:g.25918539C=	GRCh38
NC_000006.11:g.25918767C= , CM000668.1:g.25918767C=	GRCh37
NC_000006.10:g.26026746C=	NCBI36
NG_034000.1:g.17188G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377850.8:c.597G= MANE Select	ENSP00000367081.3:p.Val199=
ENST00000265425.3:c.597G=	ENSP00000265425.3:p.Val199=
ENST00000360488.7:c.597G=	ENSP00000353677.3:p.Val199=
ENST00000377850.7:c.597G=	ENSP00000367081.3:p.Val199=
NM_001286123.1:c.597G=	NP_001273052.1:p.Val199=
NM_001286125.1:c.597G=	NP_001273054.1:p.Val199=
NM_005835.3:c.597G=	NP_005826.1:p.Val199=
XM_005248784.2:c.597G=	XP_005248841.1:p.Val199=
XM_006714949.2:c.597G=	XP_006715012.1:p.Val199=
XM_006714950.1:c.528G=	XP_006715013.1:p.Val176=
XM_006714951.1:c.597G=	XP_006715014.1:p.Val199=
XM_011514227.1:c.597G=	XP_011512529.1:p.Val199=
XM_006714949.3:c.597G=	XP_006715012.1:p.Val199=
XM_006714950.2:c.528G=	XP_006715013.1:p.Val176=
XM_017010159.1:c.528G=	XP_016865648.1:p.Val176=
XM_017010160.1:c.597G=	XP_016865649.1:p.Val199=
NM_001286123.3:c.597G= MANE Select	NP_001273052.1:p.Val199=
NM_001286125.2:c.597G=	NP_001273054.1:p.Val199=
NM_005835.4:c.597G=	NP_005826.1:p.Val199=