Canonical Allele Identifier: CA2428428760

Gene: SLC35A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48904739C= , CM000685.2:g.48904739C=	GRCh38
NC_000023.10:g.48762016C= , CM000685.1:g.48762016C=	GRCh37
NC_000023.9:g.48646960C=	NCBI36
NG_015967.1:g.11822C=
NG_034300.1:g.12220G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.1163+7G= MANE Select	ENSP00000247138.5:n.1163+7G=
ENST00000247138.10:c.1163+7G=	ENSP00000247138.5:n.1163+7G=
ENST00000376515.8:c.508G=	ENSP00000365698.3:p.Ala170=
ENST00000376521.6:c.1170G=	ENSP00000365704.1:p.Val390=
ENST00000376529.8:c.573+7G=	ENSP00000365712.3:n.573+7G=
ENST00000413561.7:c.732G=
ENST00000445167.7:c.580G=	ENSP00000402726.2:p.Ala194=
ENST00000452555.7:c.1254G=	ENSP00000416002.2:p.Val418=
ENST00000616181.5:c.1209G=	ENSP00000478617.1:p.Val403=
ENST00000635285.1:c.1170G=	ENSP00000489484.1:p.Val390=
ENST00000635460.1:c.425-1274G=
ENST00000635589.1:c.987G=	ENSP00000489197.1:p.Val329=
ENST00000635628.1:c.*1064G=	ENSP00000489613.1:n.*1064G=
NM_001032289.2:c.580G=	NP_001027460.1:p.Ala194=
NM_001042498.2:c.1170G=	NP_001035963.1:p.Val390=
NM_001282647.1:c.573+7G=	NP_001269576.1:n.573+7G=
NM_001282648.1:c.508G=	NP_001269577.1:p.Ala170=
NM_001282649.1:c.987G=	NP_001269578.1:p.Val329=
NM_001282650.1:c.1209G=	NP_001269579.1:p.Val403=
NM_001282651.1:c.1254G=	NP_001269580.1:p.Val418=
NM_005660.2:c.1163+7G=	NP_005651.1:n.1163+7G=
NM_005660.3:c.1163+7G= MANE Select	NP_005651.1:n.1163+7G=
NM_001032289.3:c.580G=	NP_001027460.1:p.Ala194=
NM_001042498.3:c.1170G=	NP_001035963.1:p.Val390=
NM_001282647.2:c.573+7G=	NP_001269576.1:n.573+7G=
NM_001282649.2:c.987G=	NP_001269578.1:p.Val329=
NM_001282650.2:c.1209G=	NP_001269579.1:p.Val403=
NM_001282651.2:c.1254G=	NP_001269580.1:p.Val418=
NM_001282648.2:c.508G=	NP_001269577.1:p.Ala170=