Canonical Allele Identifier: CA412894123

Gene: SLC35A2

Linked Data

• MyVariant Identifiers: chrX:g.48762089C>A (hg19) ; chrX:g.48904812C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48904812C>A , CM000685.2:g.48904812C>A	GRCh38
NC_000023.10:g.48762089C>A , CM000685.1:g.48762089C>A	GRCh37
NC_000023.9:g.48647033C>A	NCBI36
NG_015967.1:g.11895C>A
NG_034300.1:g.12147G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.1097G>T MANE Select	ENSP00000247138.5:p.Gly366Val
ENST00000247138.10:c.1097G>T	ENSP00000247138.5:p.Gly366Val
ENST00000376515.8:c.435G>T	ENSP00000365698.3:p.Arg145=
ENST00000376521.6:c.1097G>T	ENSP00000365704.1:p.Gly366Val
ENST00000376529.8:c.507G>T	ENSP00000365712.3:p.Arg169=
ENST00000413561.7:c.659G>T
ENST00000445167.7:c.507G>T	ENSP00000402726.2:p.Arg169=
ENST00000452555.7:c.1181G>T	ENSP00000416002.2:p.Gly394Val
ENST00000616181.5:c.1136G>T	ENSP00000478617.1:p.Gly379Val
ENST00000635285.1:c.1097G>T	ENSP00000489484.1:p.Gly366Val
ENST00000635460.1:c.425-1347G>T
ENST00000635589.1:c.914G>T	ENSP00000489197.1:p.Gly305Val
ENST00000635628.1:c.*991G>T	ENSP00000489613.1:n.*991G>T
NM_001032289.2:c.507G>T	NP_001027460.1:p.Arg169=
NM_001042498.2:c.1097G>T	NP_001035963.1:p.Gly366Val
NM_001282647.1:c.507G>T	NP_001269576.1:p.Arg169=
NM_001282648.1:c.435G>T	NP_001269577.1:p.Arg145=
NM_001282649.1:c.914G>T	NP_001269578.1:p.Gly305Val
NM_001282650.1:c.1136G>T	NP_001269579.1:p.Gly379Val
NM_001282651.1:c.1181G>T	NP_001269580.1:p.Gly394Val
NM_005660.2:c.1097G>T	NP_005651.1:p.Gly366Val
NM_005660.3:c.1097G>T MANE Select	NP_005651.1:p.Gly366Val
NM_001032289.3:c.507G>T	NP_001027460.1:p.Arg169=
NM_001042498.3:c.1097G>T	NP_001035963.1:p.Gly366Val
NM_001282647.2:c.507G>T	NP_001269576.1:p.Arg169=
NM_001282649.2:c.914G>T	NP_001269578.1:p.Gly305Val
NM_001282650.2:c.1136G>T	NP_001269579.1:p.Gly379Val
NM_001282651.2:c.1181G>T	NP_001269580.1:p.Gly394Val
NM_001282648.2:c.435G>T	NP_001269577.1:p.Arg145=