Canonical Allele Identifier: CA412895821

Gene: SLC35A2

Linked Data

• MyVariant Identifiers: chrX:g.48762680C>G (hg19) ; chrX:g.48905403C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48905403C>G , CM000685.2:g.48905403C>G	GRCh38
NC_000023.10:g.48762680C>G , CM000685.1:g.48762680C>G	GRCh37
NC_000023.9:g.48647624C>G	NCBI36
NG_034300.1:g.11556G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000247138.11:c.506G>C MANE Select	ENSP00000247138.5:p.Trp169Ser
ENST00000247138.10:c.506G>C	ENSP00000247138.5:p.Trp169Ser
ENST00000376515.8:c.355-511G>C	ENSP00000365698.3:n.355-511G>C
ENST00000376521.6:c.506G>C	ENSP00000365704.1:p.Trp169Ser
ENST00000376529.8:c.427-511G>C	ENSP00000365712.3:n.427-511G>C
ENST00000413561.7:c.212-144G>C
ENST00000445167.7:c.427-511G>C	ENSP00000402726.2:n.427-511G>C
ENST00000446885.1:c.290G>C	ENSP00000415518.1:p.Trp97Ser
ENST00000452555.7:c.590G>C	ENSP00000416002.2:p.Trp197Ser
ENST00000616181.5:c.545G>C	ENSP00000478617.1:p.Trp182Ser
ENST00000634665.1:c.*126G>C	ENSP00000489356.1:n.*126G>C
ENST00000635238.1:c.467G>C	ENSP00000489515.1:p.Trp156Ser
ENST00000635285.1:c.506G>C	ENSP00000489484.1:p.Trp169Ser
ENST00000635460.1:c.424+989G>C
ENST00000635589.1:c.323G>C	ENSP00000489197.1:p.Trp108Ser
ENST00000635628.1:c.*400G>C	ENSP00000489613.1:n.*400G>C
NM_001032289.2:c.427-511G>C	NP_001027460.1:n.427-511G>C
NM_001042498.2:c.506G>C	NP_001035963.1:p.Trp169Ser
NM_001282647.1:c.427-511G>C	NP_001269576.1:n.427-511G>C
NM_001282648.1:c.355-511G>C	NP_001269577.1:n.355-511G>C
NM_001282649.1:c.323G>C	NP_001269578.1:p.Trp108Ser
NM_001282650.1:c.545G>C	NP_001269579.1:p.Trp182Ser
NM_001282651.1:c.590G>C	NP_001269580.1:p.Trp197Ser
NM_005660.2:c.506G>C	NP_005651.1:p.Trp169Ser
NM_005660.3:c.506G>C MANE Select	NP_005651.1:p.Trp169Ser
NM_001032289.3:c.427-511G>C	NP_001027460.1:n.427-511G>C
NM_001042498.3:c.506G>C	NP_001035963.1:p.Trp169Ser
NM_001282647.2:c.427-511G>C	NP_001269576.1:n.427-511G>C
NM_001282649.2:c.323G>C	NP_001269578.1:p.Trp108Ser
NM_001282650.2:c.545G>C	NP_001269579.1:p.Trp182Ser
NM_001282651.2:c.590G>C	NP_001269580.1:p.Trp197Ser
NM_001282648.2:c.355-511G>C	NP_001269577.1:n.355-511G>C