Canonical Allele Identifier: CA412895926

Gene: SLC35A2

Linked Data

• MyVariant Identifiers: chrX:g.48762731G>C (hg19) ; chrX:g.48905454G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48905454G>C , CM000685.2:g.48905454G>C	GRCh38
NC_000023.10:g.48762731G>C , CM000685.1:g.48762731G>C	GRCh37
NC_000023.9:g.48647675G>C	NCBI36
NG_034300.1:g.11505C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.455C>G MANE Select	ENSP00000247138.5:p.Thr152Arg
ENST00000247138.10:c.455C>G	ENSP00000247138.5:p.Thr152Arg
ENST00000376515.8:c.355-562C>G	ENSP00000365698.3:n.355-562C>G
ENST00000376521.6:c.455C>G	ENSP00000365704.1:p.Thr152Arg
ENST00000376529.8:c.427-562C>G	ENSP00000365712.3:n.427-562C>G
ENST00000413561.7:c.212-195C>G
ENST00000445167.7:c.427-562C>G	ENSP00000402726.2:n.427-562C>G
ENST00000446885.1:c.239C>G	ENSP00000415518.1:p.Thr80Arg
ENST00000452555.7:c.539C>G	ENSP00000416002.2:p.Thr180Arg
ENST00000616181.5:c.494C>G	ENSP00000478617.1:p.Thr165Arg
ENST00000634665.1:c.*75C>G	ENSP00000489356.1:n.*75C>G
ENST00000635238.1:c.416C>G	ENSP00000489515.1:p.Thr139Arg
ENST00000635285.1:c.455C>G	ENSP00000489484.1:p.Thr152Arg
ENST00000635460.1:c.424+938C>G
ENST00000635589.1:c.272C>G	ENSP00000489197.1:p.Thr91Arg
ENST00000635628.1:c.*349C>G	ENSP00000489613.1:n.*349C>G
NM_001032289.2:c.427-562C>G	NP_001027460.1:n.427-562C>G
NM_001042498.2:c.455C>G	NP_001035963.1:p.Thr152Arg
NM_001282647.1:c.427-562C>G	NP_001269576.1:n.427-562C>G
NM_001282648.1:c.355-562C>G	NP_001269577.1:n.355-562C>G
NM_001282649.1:c.272C>G	NP_001269578.1:p.Thr91Arg
NM_001282650.1:c.494C>G	NP_001269579.1:p.Thr165Arg
NM_001282651.1:c.539C>G	NP_001269580.1:p.Thr180Arg
NM_005660.2:c.455C>G	NP_005651.1:p.Thr152Arg
NM_005660.3:c.455C>G MANE Select	NP_005651.1:p.Thr152Arg
NM_001032289.3:c.427-562C>G	NP_001027460.1:n.427-562C>G
NM_001042498.3:c.455C>G	NP_001035963.1:p.Thr152Arg
NM_001282647.2:c.427-562C>G	NP_001269576.1:n.427-562C>G
NM_001282649.2:c.272C>G	NP_001269578.1:p.Thr91Arg
NM_001282650.2:c.494C>G	NP_001269579.1:p.Thr165Arg
NM_001282651.2:c.539C>G	NP_001269580.1:p.Thr180Arg
NM_001282648.2:c.355-562C>G	NP_001269577.1:n.355-562C>G