Canonical Allele Identifier: CA448980369

Gene: SLC17A1

Linked Data

• MyVariant Identifiers: chr6:g.25813155A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812927A>T , CM000668.2:g.25812927A>T	GRCh38
NC_000006.11:g.25813155A>T , CM000668.1:g.25813155A>T	GRCh37
NC_000006.10:g.25921134A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.801T>A MANE Select	ENSP00000244527.4:p.Ile267=
ENST00000244527.8:c.801T>A	ENSP00000244527.4:p.Ile267=
ENST00000377886.6:c.*52T>A	ENSP00000367118.2:n.*52T>A
ENST00000468082.1:c.735+168T>A	ENSP00000420546.1:n.735+168T>A
ENST00000476801.5:c.801T>A	ENSP00000420614.1:p.Ile267=
NM_005074.3:c.801T>A	NP_005065.2:p.Ile267=
XM_011514818.1:c.801T>A	XP_011513120.1:p.Ile267=
XM_011514819.1:c.714T>A	XP_011513121.1:p.Ile238=
XM_011514820.1:c.735+168T>A	XP_011513122.1:n.735+168T>A
XM_011514821.1:c.588T>A	XP_011513123.1:p.Ile196=
XM_011514818.2:c.951T>A	XP_011513120.2:p.Ile317=
XM_011514819.2:c.864T>A	XP_011513121.2:p.Ile288=
XM_011514820.2:c.885+168T>A	XP_011513122.2:n.885+168T>A
XM_011514821.2:c.588T>A	XP_011513123.1:p.Ile196=
XM_017011199.1:c.951T>A	XP_016866688.1:p.Ile317=
XM_017011200.1:c.951T>A	XP_016866689.1:p.Ile317=
XM_017011201.2:c.951T>A	XP_016866690.1:p.Ile317=
XM_017011202.1:c.867T>A	XP_016866691.1:p.Ile289=
NM_005074.5:c.801T>A MANE Select	NP_005065.2:p.Ile267=