Canonical Allele Identifier: CA2044020426

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746808G= , CM000674.2:g.68746808G=	GRCh38
NC_000012.11:g.69140588G= , CM000674.1:g.69140588G=	GRCh37
NC_000012.10:g.67426855G=	NCBI36
NG_046600.2:g.64858G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.645+29G=
ENST00000398004.4:c.402+29G= MANE Select	ENSP00000381089.2:n.402+29G=
ENST00000673712.1:c.402+29G=	ENSP00000501065.1:n.402+29G=
ENST00000674096.1:c.402+29G=	ENSP00000501130.1:n.402+29G=
ENST00000398004.3:c.402+29G=	ENSP00000381089.2:n.402+29G=
NM_018656.2:c.402+29G=	NP_061126.2:n.402+29G=
XM_005269006.2:c.402+29G=	XP_005269063.1:n.402+29G=
NM_001354997.1:c.402+29G=	NP_001341926.1:n.402+29G=
NM_001354998.1:c.402+29G=	NP_001341927.1:n.402+29G=
NM_018656.3:c.402+29G=	NP_061126.2:n.402+29G=
NR_149143.1:n.694+29G=
NR_149144.1:n.694+29G=
NM_001354997.3:c.402+29G=	NP_001341926.1:n.402+29G=
NM_001354998.2:c.402+29G=	NP_001341927.1:n.402+29G=
NM_018656.5:c.402+29G= MANE Select	NP_061126.2:n.402+29G=
NR_149143.3:n.604+29G=
NR_149144.3:n.604+29G=