Canonical Allele Identifier: CA412895979

Gene: SLC35A2

Linked Data

• MyVariant Identifiers: chrX:g.48762753A>G (hg19) ; chrX:g.48905476A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48905476A>G , CM000685.2:g.48905476A>G	GRCh38
NC_000023.10:g.48762753A>G , CM000685.1:g.48762753A>G	GRCh37
NC_000023.9:g.48647697A>G	NCBI36
NG_034300.1:g.11483T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000247138.11:c.433T>C MANE Select	ENSP00000247138.5:p.Tyr145His
ENST00000247138.10:c.433T>C	ENSP00000247138.5:p.Tyr145His
ENST00000376515.8:c.355-584T>C	ENSP00000365698.3:n.355-584T>C
ENST00000376521.6:c.433T>C	ENSP00000365704.1:p.Tyr145His
ENST00000376529.8:c.427-584T>C	ENSP00000365712.3:n.427-584T>C
ENST00000413561.7:c.212-217T>C
ENST00000445167.7:c.427-584T>C	ENSP00000402726.2:n.427-584T>C
ENST00000446885.1:c.217T>C	ENSP00000415518.1:p.Tyr73His
ENST00000452555.7:c.517T>C	ENSP00000416002.2:p.Tyr173His
ENST00000616181.5:c.472T>C	ENSP00000478617.1:p.Tyr158His
ENST00000634665.1:c.*53T>C	ENSP00000489356.1:n.*53T>C
ENST00000635238.1:c.394T>C	ENSP00000489515.1:p.Tyr132His
ENST00000635285.1:c.433T>C	ENSP00000489484.1:p.Tyr145His
ENST00000635460.1:c.424+916T>C
ENST00000635589.1:c.250T>C	ENSP00000489197.1:p.Tyr84His
ENST00000635628.1:c.*327T>C	ENSP00000489613.1:n.*327T>C
NM_001032289.2:c.427-584T>C	NP_001027460.1:n.427-584T>C
NM_001042498.2:c.433T>C	NP_001035963.1:p.Tyr145His
NM_001282647.1:c.427-584T>C	NP_001269576.1:n.427-584T>C
NM_001282648.1:c.355-584T>C	NP_001269577.1:n.355-584T>C
NM_001282649.1:c.250T>C	NP_001269578.1:p.Tyr84His
NM_001282650.1:c.472T>C	NP_001269579.1:p.Tyr158His
NM_001282651.1:c.517T>C	NP_001269580.1:p.Tyr173His
NM_005660.2:c.433T>C	NP_005651.1:p.Tyr145His
NM_005660.3:c.433T>C MANE Select	NP_005651.1:p.Tyr145His
NM_001032289.3:c.427-584T>C	NP_001027460.1:n.427-584T>C
NM_001042498.3:c.433T>C	NP_001035963.1:p.Tyr145His
NM_001282647.2:c.427-584T>C	NP_001269576.1:n.427-584T>C
NM_001282649.2:c.250T>C	NP_001269578.1:p.Tyr84His
NM_001282650.2:c.472T>C	NP_001269579.1:p.Tyr158His
NM_001282651.2:c.517T>C	NP_001269580.1:p.Tyr173His
NM_001282648.2:c.355-584T>C	NP_001269577.1:n.355-584T>C