Canonical Allele Identifier: CA363158090

Gene: SLC17A1

Linked Data

• MyVariant Identifiers: chr6:g.25813160C>G (hg19) ; chr6:g.25812932C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812932C>G , CM000668.2:g.25812932C>G	GRCh38
NC_000006.11:g.25813160C>G , CM000668.1:g.25813160C>G	GRCh37
NC_000006.10:g.25921139C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244527.10:c.796G>C MANE Select	ENSP00000244527.4:p.Ala266Pro
ENST00000244527.8:c.796G>C	ENSP00000244527.4:p.Ala266Pro
ENST00000377886.6:c.*47G>C	ENSP00000367118.2:n.*47G>C
ENST00000468082.1:c.735+163G>C	ENSP00000420546.1:n.735+163G>C
ENST00000476801.5:c.796G>C	ENSP00000420614.1:p.Ala266Pro
NM_005074.3:c.796G>C	NP_005065.2:p.Ala266Pro
XM_011514818.1:c.796G>C	XP_011513120.1:p.Ala266Pro
XM_011514819.1:c.709G>C	XP_011513121.1:p.Ala237Pro
XM_011514820.1:c.735+163G>C	XP_011513122.1:n.735+163G>C
XM_011514821.1:c.583G>C	XP_011513123.1:p.Ala195Pro
XM_011514818.2:c.946G>C	XP_011513120.2:p.Ala316Pro
XM_011514819.2:c.859G>C	XP_011513121.2:p.Ala287Pro
XM_011514820.2:c.885+163G>C	XP_011513122.2:n.885+163G>C
XM_011514821.2:c.583G>C	XP_011513123.1:p.Ala195Pro
XM_017011199.1:c.946G>C	XP_016866688.1:p.Ala316Pro
XM_017011200.1:c.946G>C	XP_016866689.1:p.Ala316Pro
XM_017011201.2:c.946G>C	XP_016866690.1:p.Ala316Pro
XM_017011202.1:c.862G>C	XP_016866691.1:p.Ala288Pro
NM_005074.5:c.796G>C MANE Select	NP_005065.2:p.Ala266Pro