Canonical Allele Identifier: CA2044020185

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746701C= , CM000674.2:g.68746701C=	GRCh38
NC_000012.11:g.69140481C= , CM000674.1:g.69140481C=	GRCh37
NC_000012.10:g.67426748C=	NCBI36
NG_046600.2:g.64751C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.567C=
ENST00000398004.4:c.324C= MANE Select	ENSP00000381089.2:p.Ala108=
ENST00000673712.1:c.324C=	ENSP00000501065.1:p.Ala108=
ENST00000674096.1:c.324C=	ENSP00000501130.1:p.Ala108=
ENST00000398004.3:c.324C=	ENSP00000381089.2:p.Ala108=
NM_018656.2:c.324C=	NP_061126.2:p.Ala108=
XM_005269006.2:c.324C=	XP_005269063.1:p.Ala108=
NM_001354997.1:c.324C=	NP_001341926.1:p.Ala108=
NM_001354998.1:c.324C=	NP_001341927.1:p.Ala108=
NM_018656.3:c.324C=	NP_061126.2:p.Ala108=
NR_149143.1:n.616C=
NR_149144.1:n.616C=
NM_001354997.3:c.324C=	NP_001341926.1:p.Ala108=
NM_001354998.2:c.324C=	NP_001341927.1:p.Ala108=
NM_018656.5:c.324C= MANE Select	NP_061126.2:p.Ala108=
NR_149143.3:n.526C=
NR_149144.3:n.526C=