Canonical Allele Identifier: CA2428428840

Gene: SLC35A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48904970A= , CM000685.2:g.48904970A=	GRCh38
NC_000023.10:g.48762247A= , CM000685.1:g.48762247A=	GRCh37
NC_000023.9:g.48647191A=	NCBI36
NG_015967.1:g.12053A=
NG_034300.1:g.11989T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247138.11:c.939T= MANE Select	ENSP00000247138.5:p.Ile313=
ENST00000247138.10:c.939T=	ENSP00000247138.5:p.Ile313=
ENST00000376515.8:c.355-78T=	ENSP00000365698.3:n.355-78T=
ENST00000376521.6:c.939T=	ENSP00000365704.1:p.Ile313=
ENST00000376529.8:c.427-78T=	ENSP00000365712.3:n.427-78T=
ENST00000413561.7:c.501T=
ENST00000445167.7:c.427-78T=	ENSP00000402726.2:n.427-78T=
ENST00000452555.7:c.1023T=	ENSP00000416002.2:p.Ile341=
ENST00000616181.5:c.978T=	ENSP00000478617.1:p.Ile326=
ENST00000635285.1:c.939T=	ENSP00000489484.1:p.Ile313=
ENST00000635460.1:c.424+1422T=
ENST00000635589.1:c.756T=	ENSP00000489197.1:p.Ile252=
ENST00000635628.1:c.*833T=	ENSP00000489613.1:n.*833T=
NM_001032289.2:c.427-78T=	NP_001027460.1:n.427-78T=
NM_001042498.2:c.939T=	NP_001035963.1:p.Ile313=
NM_001282647.1:c.427-78T=	NP_001269576.1:n.427-78T=
NM_001282648.1:c.355-78T=	NP_001269577.1:n.355-78T=
NM_001282649.1:c.756T=	NP_001269578.1:p.Ile252=
NM_001282650.1:c.978T=	NP_001269579.1:p.Ile326=
NM_001282651.1:c.1023T=	NP_001269580.1:p.Ile341=
NM_005660.2:c.939T=	NP_005651.1:p.Ile313=
NM_005660.3:c.939T= MANE Select	NP_005651.1:p.Ile313=
NM_001032289.3:c.427-78T=	NP_001027460.1:n.427-78T=
NM_001042498.3:c.939T=	NP_001035963.1:p.Ile313=
NM_001282647.2:c.427-78T=	NP_001269576.1:n.427-78T=
NM_001282649.2:c.756T=	NP_001269578.1:p.Ile252=
NM_001282650.2:c.978T=	NP_001269579.1:p.Ile326=
NM_001282651.2:c.1023T=	NP_001269580.1:p.Ile341=
NM_001282648.2:c.355-78T=	NP_001269577.1:n.355-78T=