Canonical Allele Identifier: CA2428428771

Gene: SLC35A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48904780G= , CM000685.2:g.48904780G=	GRCh38
NC_000023.10:g.48762057G= , CM000685.1:g.48762057G=	GRCh37
NC_000023.9:g.48647001G=	NCBI36
NG_015967.1:g.11863G=
NG_034300.1:g.12179C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.1129C= MANE Select	ENSP00000247138.5:p.Arg377=
ENST00000247138.10:c.1129C=	ENSP00000247138.5:p.Arg377=
ENST00000376515.8:c.467C=	ENSP00000365698.3:p.Pro156=
ENST00000376521.6:c.1129C=	ENSP00000365704.1:p.Arg377=
ENST00000376529.8:c.539C=	ENSP00000365712.3:p.Pro180=
ENST00000413561.7:c.691C=
ENST00000445167.7:c.539C=	ENSP00000402726.2:p.Pro180=
ENST00000452555.7:c.1213C=	ENSP00000416002.2:p.Arg405=
ENST00000616181.5:c.1168C=	ENSP00000478617.1:p.Arg390=
ENST00000635285.1:c.1129C=	ENSP00000489484.1:p.Arg377=
ENST00000635460.1:c.425-1315C=
ENST00000635589.1:c.946C=	ENSP00000489197.1:p.Arg316=
ENST00000635628.1:c.*1023C=	ENSP00000489613.1:n.*1023C=
NM_001032289.2:c.539C=	NP_001027460.1:p.Pro180=
NM_001042498.2:c.1129C=	NP_001035963.1:p.Arg377=
NM_001282647.1:c.539C=	NP_001269576.1:p.Pro180=
NM_001282648.1:c.467C=	NP_001269577.1:p.Pro156=
NM_001282649.1:c.946C=	NP_001269578.1:p.Arg316=
NM_001282650.1:c.1168C=	NP_001269579.1:p.Arg390=
NM_001282651.1:c.1213C=	NP_001269580.1:p.Arg405=
NM_005660.2:c.1129C=	NP_005651.1:p.Arg377=
NM_005660.3:c.1129C= MANE Select	NP_005651.1:p.Arg377=
NM_001032289.3:c.539C=	NP_001027460.1:p.Pro180=
NM_001042498.3:c.1129C=	NP_001035963.1:p.Arg377=
NM_001282647.2:c.539C=	NP_001269576.1:p.Pro180=
NM_001282649.2:c.946C=	NP_001269578.1:p.Arg316=
NM_001282650.2:c.1168C=	NP_001269579.1:p.Arg390=
NM_001282651.2:c.1213C=	NP_001269580.1:p.Arg405=
NM_001282648.2:c.467C=	NP_001269577.1:p.Pro156=