Canonical Allele Identifier: CA1616765662

Gene: SLC17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812996G= , CM000668.2:g.25812996G=	GRCh38
NC_000006.11:g.25813224G= , CM000668.1:g.25813224G=	GRCh37
NC_000006.10:g.25921203G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.736-4C= MANE Select	ENSP00000244527.4:n.736-4C=
ENST00000244527.8:c.736-4C=	ENSP00000244527.4:n.736-4C=
ENST00000377886.6:c.617-4C=	ENSP00000367118.2:n.617-4C=
ENST00000468082.1:c.735+99C=	ENSP00000420546.1:n.735+99C=
ENST00000476801.5:c.736-4C=	ENSP00000420614.1:n.736-4C=
NM_005074.3:c.736-4C=	NP_005065.2:n.736-4C=
XM_011514818.1:c.736-4C=	XP_011513120.1:n.736-4C=
XM_011514819.1:c.649-4C=	XP_011513121.1:n.649-4C=
XM_011514820.1:c.735+99C=	XP_011513122.1:n.735+99C=
XM_011514821.1:c.523-4C=	XP_011513123.1:n.523-4C=
XM_011514818.2:c.886-4C=	XP_011513120.2:n.886-4C=
XM_011514819.2:c.799-4C=	XP_011513121.2:n.799-4C=
XM_011514820.2:c.885+99C=	XP_011513122.2:n.885+99C=
XM_011514821.2:c.523-4C=	XP_011513123.1:n.523-4C=
XM_017011199.1:c.886-4C=	XP_016866688.1:n.886-4C=
XM_017011200.1:c.886-4C=	XP_016866689.1:n.886-4C=
XM_017011201.2:c.886-4C=	XP_016866690.1:n.886-4C=
XM_017011202.1:c.802-4C=	XP_016866691.1:n.802-4C=
NM_005074.5:c.736-4C= MANE Select	NP_005065.2:n.736-4C=