Canonical Allele Identifier: CA2428428966

Gene: SLC35A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48905412C= , CM000685.2:g.48905412C=	GRCh38
NC_000023.10:g.48762689C= , CM000685.1:g.48762689C=	GRCh37
NC_000023.9:g.48647633C=	NCBI36
NG_034300.1:g.11547G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000247138.11:c.497G= MANE Select	ENSP00000247138.5:p.Arg166=
ENST00000247138.10:c.497G=	ENSP00000247138.5:p.Arg166=
ENST00000376515.8:c.355-520G=	ENSP00000365698.3:n.355-520G=
ENST00000376521.6:c.497G=	ENSP00000365704.1:p.Arg166=
ENST00000376529.8:c.427-520G=	ENSP00000365712.3:n.427-520G=
ENST00000413561.7:c.212-153G=
ENST00000445167.7:c.427-520G=	ENSP00000402726.2:n.427-520G=
ENST00000446885.1:c.281G=	ENSP00000415518.1:p.Arg94=
ENST00000452555.7:c.581G=	ENSP00000416002.2:p.Arg194=
ENST00000616181.5:c.536G=	ENSP00000478617.1:p.Arg179=
ENST00000634665.1:c.*117G=	ENSP00000489356.1:n.*117G=
ENST00000635238.1:c.458G=	ENSP00000489515.1:p.Arg153=
ENST00000635285.1:c.497G=	ENSP00000489484.1:p.Arg166=
ENST00000635460.1:c.424+980G=
ENST00000635589.1:c.314G=	ENSP00000489197.1:p.Arg105=
ENST00000635628.1:c.*391G=	ENSP00000489613.1:n.*391G=
NM_001032289.2:c.427-520G=	NP_001027460.1:n.427-520G=
NM_001042498.2:c.497G=	NP_001035963.1:p.Arg166=
NM_001282647.1:c.427-520G=	NP_001269576.1:n.427-520G=
NM_001282648.1:c.355-520G=	NP_001269577.1:n.355-520G=
NM_001282649.1:c.314G=	NP_001269578.1:p.Arg105=
NM_001282650.1:c.536G=	NP_001269579.1:p.Arg179=
NM_001282651.1:c.581G=	NP_001269580.1:p.Arg194=
NM_005660.2:c.497G=	NP_005651.1:p.Arg166=
NM_005660.3:c.497G= MANE Select	NP_005651.1:p.Arg166=
NM_001032289.3:c.427-520G=	NP_001027460.1:n.427-520G=
NM_001042498.3:c.497G=	NP_001035963.1:p.Arg166=
NM_001282647.2:c.427-520G=	NP_001269576.1:n.427-520G=
NM_001282649.2:c.314G=	NP_001269578.1:p.Arg105=
NM_001282650.2:c.536G=	NP_001269579.1:p.Arg179=
NM_001282651.2:c.581G=	NP_001269580.1:p.Arg194=
NM_001282648.2:c.355-520G=	NP_001269577.1:n.355-520G=