Canonical Allele Identifier: CA2428428926

Gene: SLC35A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48905294G= , CM000685.2:g.48905294G=	GRCh38
NC_000023.10:g.48762571G= , CM000685.1:g.48762571G=	GRCh37
NC_000023.9:g.48647515G=	NCBI36
NG_034300.1:g.11665C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000247138.11:c.615C= MANE Select	ENSP00000247138.5:p.Ala205=
ENST00000247138.10:c.615C=	ENSP00000247138.5:p.Ala205=
ENST00000376515.8:c.355-402C=	ENSP00000365698.3:n.355-402C=
ENST00000376521.6:c.615C=	ENSP00000365704.1:p.Ala205=
ENST00000376529.8:c.427-402C=	ENSP00000365712.3:n.427-402C=
ENST00000413561.7:c.212-35C=
ENST00000445167.7:c.427-402C=	ENSP00000402726.2:n.427-402C=
ENST00000446885.1:c.399C=	ENSP00000415518.1:p.Ala133=
ENST00000452555.7:c.699C=	ENSP00000416002.2:p.Ala233=
ENST00000616181.5:c.654C=	ENSP00000478617.1:p.Ala218=
ENST00000635285.1:c.615C=	ENSP00000489484.1:p.Ala205=
ENST00000635460.1:c.424+1098C=
ENST00000635589.1:c.432C=	ENSP00000489197.1:p.Ala144=
ENST00000635628.1:c.*509C=	ENSP00000489613.1:n.*509C=
NM_001032289.2:c.427-402C=	NP_001027460.1:n.427-402C=
NM_001042498.2:c.615C=	NP_001035963.1:p.Ala205=
NM_001282647.1:c.427-402C=	NP_001269576.1:n.427-402C=
NM_001282648.1:c.355-402C=	NP_001269577.1:n.355-402C=
NM_001282649.1:c.432C=	NP_001269578.1:p.Ala144=
NM_001282650.1:c.654C=	NP_001269579.1:p.Ala218=
NM_001282651.1:c.699C=	NP_001269580.1:p.Ala233=
NM_005660.2:c.615C=	NP_005651.1:p.Ala205=
NM_005660.3:c.615C= MANE Select	NP_005651.1:p.Ala205=
NM_001032289.3:c.427-402C=	NP_001027460.1:n.427-402C=
NM_001042498.3:c.615C=	NP_001035963.1:p.Ala205=
NM_001282647.2:c.427-402C=	NP_001269576.1:n.427-402C=
NM_001282649.2:c.432C=	NP_001269578.1:p.Ala144=
NM_001282650.2:c.654C=	NP_001269579.1:p.Ala218=
NM_001282651.2:c.699C=	NP_001269580.1:p.Ala233=
NM_001282648.2:c.355-402C=	NP_001269577.1:n.355-402C=