Canonical Allele Identifier: CA412894203

Gene: SLC35A2

Linked Data

• MyVariant Identifiers: chrX:g.48762116C>A (hg19) ; chrX:g.48904839C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48904839C>A , CM000685.2:g.48904839C>A	GRCh38
NC_000023.10:g.48762116C>A , CM000685.1:g.48762116C>A	GRCh37
NC_000023.9:g.48647060C>A	NCBI36
NG_015967.1:g.11922C>A
NG_034300.1:g.12120G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000247138.11:c.1070G>T MANE Select	ENSP00000247138.5:p.Gly357Val
ENST00000247138.10:c.1070G>T	ENSP00000247138.5:p.Gly357Val
ENST00000376515.8:c.408G>T	ENSP00000365698.3:p.Arg136=
ENST00000376521.6:c.1070G>T	ENSP00000365704.1:p.Gly357Val
ENST00000376529.8:c.480G>T	ENSP00000365712.3:p.Arg160=
ENST00000413561.7:c.632G>T
ENST00000445167.7:c.480G>T	ENSP00000402726.2:p.Arg160=
ENST00000452555.7:c.1154G>T	ENSP00000416002.2:p.Gly385Val
ENST00000616181.5:c.1109G>T	ENSP00000478617.1:p.Gly370Val
ENST00000635285.1:c.1070G>T	ENSP00000489484.1:p.Gly357Val
ENST00000635460.1:c.425-1374G>T
ENST00000635589.1:c.887G>T	ENSP00000489197.1:p.Gly296Val
ENST00000635628.1:c.*964G>T	ENSP00000489613.1:n.*964G>T
NM_001032289.2:c.480G>T	NP_001027460.1:p.Arg160=
NM_001042498.2:c.1070G>T	NP_001035963.1:p.Gly357Val
NM_001282647.1:c.480G>T	NP_001269576.1:p.Arg160=
NM_001282648.1:c.408G>T	NP_001269577.1:p.Arg136=
NM_001282649.1:c.887G>T	NP_001269578.1:p.Gly296Val
NM_001282650.1:c.1109G>T	NP_001269579.1:p.Gly370Val
NM_001282651.1:c.1154G>T	NP_001269580.1:p.Gly385Val
NM_005660.2:c.1070G>T	NP_005651.1:p.Gly357Val
NM_005660.3:c.1070G>T MANE Select	NP_005651.1:p.Gly357Val
NM_001032289.3:c.480G>T	NP_001027460.1:p.Arg160=
NM_001042498.3:c.1070G>T	NP_001035963.1:p.Gly357Val
NM_001282647.2:c.480G>T	NP_001269576.1:p.Arg160=
NM_001282649.2:c.887G>T	NP_001269578.1:p.Gly296Val
NM_001282650.2:c.1109G>T	NP_001269579.1:p.Gly370Val
NM_001282651.2:c.1154G>T	NP_001269580.1:p.Gly385Val
NM_001282648.2:c.408G>T	NP_001269577.1:p.Arg136=