Canonical Allele Identifier: CA363158295

Gene: SLC17A1

Linked Data

• MyVariant Identifiers: chr6:g.25813220C>T (hg19) ; chr6:g.25812992C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.25812992C>T , CM000668.2:g.25812992C>T	GRCh38
NC_000006.11:g.25813220C>T , CM000668.1:g.25813220C>T	GRCh37
NC_000006.10:g.25921199C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244527.10:c.736G>A MANE Select	ENSP00000244527.4:p.Val246Ile
ENST00000244527.8:c.736G>A	ENSP00000244527.4:p.Val246Ile
ENST00000377886.6:c.617G>A	ENSP00000367118.2:p.Gly206Asp
ENST00000468082.1:c.735+103G>A	ENSP00000420546.1:n.735+103G>A
ENST00000476801.5:c.736G>A	ENSP00000420614.1:p.Val246Ile
NM_005074.3:c.736G>A	NP_005065.2:p.Val246Ile
XM_011514818.1:c.736G>A	XP_011513120.1:p.Val246Ile
XM_011514819.1:c.649G>A	XP_011513121.1:p.Val217Ile
XM_011514820.1:c.735+103G>A	XP_011513122.1:n.735+103G>A
XM_011514821.1:c.523G>A	XP_011513123.1:p.Val175Ile
XM_011514818.2:c.886G>A	XP_011513120.2:p.Val296Ile
XM_011514819.2:c.799G>A	XP_011513121.2:p.Val267Ile
XM_011514820.2:c.885+103G>A	XP_011513122.2:n.885+103G>A
XM_011514821.2:c.523G>A	XP_011513123.1:p.Val175Ile
XM_017011199.1:c.886G>A	XP_016866688.1:p.Val296Ile
XM_017011200.1:c.886G>A	XP_016866689.1:p.Val296Ile
XM_017011201.2:c.886G>A	XP_016866690.1:p.Val296Ile
XM_017011202.1:c.802G>A	XP_016866691.1:p.Val268Ile
NM_005074.5:c.736G>A MANE Select	NP_005065.2:p.Val246Ile