Canonical Allele Identifier: CA412894013

Gene: SLC35A2

Linked Data

• MyVariant Identifiers: chrX:g.48762048G>T (hg19) ; chrX:g.48904771G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48904771G>T , CM000685.2:g.48904771G>T	GRCh38
NC_000023.10:g.48762048G>T , CM000685.1:g.48762048G>T	GRCh37
NC_000023.9:g.48646992G>T	NCBI36
NG_015967.1:g.11854G>T
NG_034300.1:g.12188C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.1138C>A MANE Select	ENSP00000247138.5:p.Leu380Ile
ENST00000247138.10:c.1138C>A	ENSP00000247138.5:p.Leu380Ile
ENST00000376515.8:c.476C>A	ENSP00000365698.3:p.Pro159His
ENST00000376521.6:c.1138C>A	ENSP00000365704.1:p.Leu380Ile
ENST00000376529.8:c.548C>A	ENSP00000365712.3:p.Pro183His
ENST00000413561.7:c.700C>A
ENST00000445167.7:c.548C>A	ENSP00000402726.2:p.Pro183His
ENST00000452555.7:c.1222C>A	ENSP00000416002.2:p.Leu408Ile
ENST00000616181.5:c.1177C>A	ENSP00000478617.1:p.Leu393Ile
ENST00000635285.1:c.1138C>A	ENSP00000489484.1:p.Leu380Ile
ENST00000635460.1:c.425-1306C>A
ENST00000635589.1:c.955C>A	ENSP00000489197.1:p.Leu319Ile
ENST00000635628.1:c.*1032C>A	ENSP00000489613.1:n.*1032C>A
NM_001032289.2:c.548C>A	NP_001027460.1:p.Pro183His
NM_001042498.2:c.1138C>A	NP_001035963.1:p.Leu380Ile
NM_001282647.1:c.548C>A	NP_001269576.1:p.Pro183His
NM_001282648.1:c.476C>A	NP_001269577.1:p.Pro159His
NM_001282649.1:c.955C>A	NP_001269578.1:p.Leu319Ile
NM_001282650.1:c.1177C>A	NP_001269579.1:p.Leu393Ile
NM_001282651.1:c.1222C>A	NP_001269580.1:p.Leu408Ile
NM_005660.2:c.1138C>A	NP_005651.1:p.Leu380Ile
NM_005660.3:c.1138C>A MANE Select	NP_005651.1:p.Leu380Ile
NM_001032289.3:c.548C>A	NP_001027460.1:p.Pro183His
NM_001042498.3:c.1138C>A	NP_001035963.1:p.Leu380Ile
NM_001282647.2:c.548C>A	NP_001269576.1:p.Pro183His
NM_001282649.2:c.955C>A	NP_001269578.1:p.Leu319Ile
NM_001282650.2:c.1177C>A	NP_001269579.1:p.Leu393Ile
NM_001282651.2:c.1222C>A	NP_001269580.1:p.Leu408Ile
NM_001282648.2:c.476C>A	NP_001269577.1:p.Pro159His