Canonical Allele Identifier: CA2428428975

Gene: SLC35A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48905450C= , CM000685.2:g.48905450C=	GRCh38
NC_000023.10:g.48762727C= , CM000685.1:g.48762727C=	GRCh37
NC_000023.9:g.48647671C=	NCBI36
NG_034300.1:g.11509G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.459G= MANE Select	ENSP00000247138.5:p.Ala153=
ENST00000247138.10:c.459G=	ENSP00000247138.5:p.Ala153=
ENST00000376515.8:c.355-558G=	ENSP00000365698.3:n.355-558G=
ENST00000376521.6:c.459G=	ENSP00000365704.1:p.Ala153=
ENST00000376529.8:c.427-558G=	ENSP00000365712.3:n.427-558G=
ENST00000413561.7:c.212-191G=
ENST00000445167.7:c.427-558G=	ENSP00000402726.2:n.427-558G=
ENST00000446885.1:c.243G=	ENSP00000415518.1:p.Ala81=
ENST00000452555.7:c.543G=	ENSP00000416002.2:p.Ala181=
ENST00000616181.5:c.498G=	ENSP00000478617.1:p.Ala166=
ENST00000634665.1:c.*79G=	ENSP00000489356.1:n.*79G=
ENST00000635238.1:c.420G=	ENSP00000489515.1:p.Ala140=
ENST00000635285.1:c.459G=	ENSP00000489484.1:p.Ala153=
ENST00000635460.1:c.424+942G=
ENST00000635589.1:c.276G=	ENSP00000489197.1:p.Ala92=
ENST00000635628.1:c.*353G=	ENSP00000489613.1:n.*353G=
NM_001032289.2:c.427-558G=	NP_001027460.1:n.427-558G=
NM_001042498.2:c.459G=	NP_001035963.1:p.Ala153=
NM_001282647.1:c.427-558G=	NP_001269576.1:n.427-558G=
NM_001282648.1:c.355-558G=	NP_001269577.1:n.355-558G=
NM_001282649.1:c.276G=	NP_001269578.1:p.Ala92=
NM_001282650.1:c.498G=	NP_001269579.1:p.Ala166=
NM_001282651.1:c.543G=	NP_001269580.1:p.Ala181=
NM_005660.2:c.459G=	NP_005651.1:p.Ala153=
NM_005660.3:c.459G= MANE Select	NP_005651.1:p.Ala153=
NM_001032289.3:c.427-558G=	NP_001027460.1:n.427-558G=
NM_001042498.3:c.459G=	NP_001035963.1:p.Ala153=
NM_001282647.2:c.427-558G=	NP_001269576.1:n.427-558G=
NM_001282649.2:c.276G=	NP_001269578.1:p.Ala92=
NM_001282650.2:c.498G=	NP_001269579.1:p.Ala166=
NM_001282651.2:c.543G=	NP_001269580.1:p.Ala181=
NM_001282648.2:c.355-558G=	NP_001269577.1:n.355-558G=