Canonical Allele Identifier: CA363158077

Gene: SLC17A1

Linked Data

• gnomAD v4: 6-25812926-A-G
• MyVariant Identifiers: chr6:g.25813154A>G (hg19) ; chr6:g.25812926A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812926A>G , CM000668.2:g.25812926A>G	GRCh38
NC_000006.11:g.25813154A>G , CM000668.1:g.25813154A>G	GRCh37
NC_000006.10:g.25921133A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244527.10:c.802T>C MANE Select	ENSP00000244527.4:p.Ser268Pro
ENST00000244527.8:c.802T>C	ENSP00000244527.4:p.Ser268Pro
ENST00000377886.6:c.*53T>C	ENSP00000367118.2:n.*53T>C
ENST00000468082.1:c.735+169T>C	ENSP00000420546.1:n.735+169T>C
ENST00000476801.5:c.802T>C	ENSP00000420614.1:p.Ser268Pro
NM_005074.3:c.802T>C	NP_005065.2:p.Ser268Pro
XM_011514818.1:c.802T>C	XP_011513120.1:p.Ser268Pro
XM_011514819.1:c.715T>C	XP_011513121.1:p.Ser239Pro
XM_011514820.1:c.735+169T>C	XP_011513122.1:n.735+169T>C
XM_011514821.1:c.589T>C	XP_011513123.1:p.Ser197Pro
XM_011514818.2:c.952T>C	XP_011513120.2:p.Ser318Pro
XM_011514819.2:c.865T>C	XP_011513121.2:p.Ser289Pro
XM_011514820.2:c.885+169T>C	XP_011513122.2:n.885+169T>C
XM_011514821.2:c.589T>C	XP_011513123.1:p.Ser197Pro
XM_017011199.1:c.952T>C	XP_016866688.1:p.Ser318Pro
XM_017011200.1:c.952T>C	XP_016866689.1:p.Ser318Pro
XM_017011201.2:c.952T>C	XP_016866690.1:p.Ser318Pro
XM_017011202.1:c.868T>C	XP_016866691.1:p.Ser290Pro
NM_005074.5:c.802T>C MANE Select	NP_005065.2:p.Ser268Pro