Canonical Allele Identifier: CA448980372

Gene: SLC17A1

Linked Data

• MyVariant Identifiers: chr6:g.25813164G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812936G>A , CM000668.2:g.25812936G>A	GRCh38
NC_000006.11:g.25813164G>A , CM000668.1:g.25813164G>A	GRCh37
NC_000006.10:g.25921143G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.792C>T MANE Select	ENSP00000244527.4:p.Val264=
ENST00000244527.8:c.792C>T	ENSP00000244527.4:p.Val264=
ENST00000377886.6:c.*43C>T	ENSP00000367118.2:n.*43C>T
ENST00000468082.1:c.735+159C>T	ENSP00000420546.1:n.735+159C>T
ENST00000476801.5:c.792C>T	ENSP00000420614.1:p.Val264=
NM_005074.3:c.792C>T	NP_005065.2:p.Val264=
XM_011514818.1:c.792C>T	XP_011513120.1:p.Val264=
XM_011514819.1:c.705C>T	XP_011513121.1:p.Val235=
XM_011514820.1:c.735+159C>T	XP_011513122.1:n.735+159C>T
XM_011514821.1:c.579C>T	XP_011513123.1:p.Val193=
XM_011514818.2:c.942C>T	XP_011513120.2:p.Val314=
XM_011514819.2:c.855C>T	XP_011513121.2:p.Val285=
XM_011514820.2:c.885+159C>T	XP_011513122.2:n.885+159C>T
XM_011514821.2:c.579C>T	XP_011513123.1:p.Val193=
XM_017011199.1:c.942C>T	XP_016866688.1:p.Val314=
XM_017011200.1:c.942C>T	XP_016866689.1:p.Val314=
XM_017011201.2:c.942C>T	XP_016866690.1:p.Val314=
XM_017011202.1:c.858C>T	XP_016866691.1:p.Val286=
NM_005074.5:c.792C>T MANE Select	NP_005065.2:p.Val264=