Canonical Allele Identifier: CA1616759585

Gene: SLC17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25798704G= , CM000668.2:g.25798704G=	GRCh38
NC_000006.11:g.25798932G= , CM000668.1:g.25798932G=	GRCh37
NC_000006.10:g.25906911G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.*2+79C= MANE Select	ENSP00000244527.4:n.*2+79C=
ENST00000244527.8:c.*2+79C=	ENSP00000244527.4:n.*2+79C=
ENST00000377886.6:c.*657+79C=	ENSP00000367118.2:n.*657+79C=
ENST00000476801.5:c.*81C=	ENSP00000420614.1:n.*81C=
NM_005074.3:c.*2+79C=	NP_005065.2:n.*2+79C=
XM_011514818.1:c.1178+12694C=	XP_011513120.1:n.1178+12694C=
XM_011514819.1:c.*81C=	XP_011513121.1:n.*81C=
XM_011514820.1:c.*81C=	XP_011513122.1:n.*81C=
XM_011514821.1:c.*81C=	XP_011513123.1:n.*81C=
XM_011514818.2:c.1328+12694C=	XP_011513120.2:n.1328+12694C=
XM_011514819.2:c.*81C=	XP_011513121.2:n.*81C=
XM_011514820.2:c.*81C=	XP_011513122.2:n.*81C=
XM_011514821.2:c.*81C=	XP_011513123.1:n.*81C=
XM_017011199.1:c.*81C=	XP_016866688.1:n.*81C=
XM_017011200.1:c.*2+79C=	XP_016866689.1:n.*2+79C=
XM_017011201.2:c.*2+79C=	XP_016866690.1:n.*2+79C=
XM_017011202.1:c.*81C=	XP_016866691.1:n.*81C=
NM_005074.5:c.*2+79C= MANE Select	NP_005065.2:n.*2+79C=