Canonical Allele Identifier: CA412895602

Gene: SLC35A2

Linked Data

• ClinVar Variation Id: 1531313
• ClinVar RCV Id: RCV002099643 ; RCV003403670
• dbSNP Id: rs2147487234
• MyVariant Identifiers: chrX:g.48762576C>T (hg19) ; chrX:g.48905299C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48905299C>T , CM000685.2:g.48905299C>T	GRCh38
NC_000023.10:g.48762576C>T , CM000685.1:g.48762576C>T	GRCh37
NC_000023.9:g.48647520C>T	NCBI36
NG_034300.1:g.11660G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000247138.11:c.610G>A MANE Select	ENSP00000247138.5:p.Ala204Thr
ENST00000247138.10:c.610G>A	ENSP00000247138.5:p.Ala204Thr
ENST00000376515.8:c.355-407G>A	ENSP00000365698.3:n.355-407G>A
ENST00000376521.6:c.610G>A	ENSP00000365704.1:p.Ala204Thr
ENST00000376529.8:c.427-407G>A	ENSP00000365712.3:n.427-407G>A
ENST00000413561.7:c.212-40G>A
ENST00000445167.7:c.427-407G>A	ENSP00000402726.2:n.427-407G>A
ENST00000446885.1:c.394G>A	ENSP00000415518.1:p.Ala132Thr
ENST00000452555.7:c.694G>A	ENSP00000416002.2:p.Ala232Thr
ENST00000616181.5:c.649G>A	ENSP00000478617.1:p.Ala217Thr
ENST00000635238.1:c.571G>A	ENSP00000489515.1:p.Ala191Thr
ENST00000635285.1:c.610G>A	ENSP00000489484.1:p.Ala204Thr
ENST00000635460.1:c.424+1093G>A
ENST00000635589.1:c.427G>A	ENSP00000489197.1:p.Ala143Thr
ENST00000635628.1:c.*504G>A	ENSP00000489613.1:n.*504G>A
NM_001032289.2:c.427-407G>A	NP_001027460.1:n.427-407G>A
NM_001042498.2:c.610G>A	NP_001035963.1:p.Ala204Thr
NM_001282647.1:c.427-407G>A	NP_001269576.1:n.427-407G>A
NM_001282648.1:c.355-407G>A	NP_001269577.1:n.355-407G>A
NM_001282649.1:c.427G>A	NP_001269578.1:p.Ala143Thr
NM_001282650.1:c.649G>A	NP_001269579.1:p.Ala217Thr
NM_001282651.1:c.694G>A	NP_001269580.1:p.Ala232Thr
NM_005660.2:c.610G>A	NP_005651.1:p.Ala204Thr
NM_005660.3:c.610G>A MANE Select	NP_005651.1:p.Ala204Thr
NM_001032289.3:c.427-407G>A	NP_001027460.1:n.427-407G>A
NM_001042498.3:c.610G>A	NP_001035963.1:p.Ala204Thr
NM_001282647.2:c.427-407G>A	NP_001269576.1:n.427-407G>A
NM_001282649.2:c.427G>A	NP_001269578.1:p.Ala143Thr
NM_001282650.2:c.649G>A	NP_001269579.1:p.Ala217Thr
NM_001282651.2:c.694G>A	NP_001269580.1:p.Ala232Thr
NM_001282648.2:c.355-407G>A	NP_001269577.1:n.355-407G>A