Canonical Allele Identifier: CA2839529156

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746381dup , CM000674.2:g.68746381dup	GRCh38
NC_000012.11:g.69140161dup , CM000674.1:g.69140161dup	GRCh37
NC_000012.10:g.67426428dup	NCBI36
NG_046600.2:g.64431dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.247dup
ENST00000398004.4:c.4dup MANE Select	ENSP00000381089.2:p.Ala2GlyfsTer?
ENST00000673712.1:c.4dup	ENSP00000501065.1:p.Ala2GlyfsTer?
ENST00000674096.1:c.4dup	ENSP00000501130.1:p.Ala2GlyfsTer?
ENST00000398004.3:c.4dup	ENSP00000381089.2:p.Ala2GlyfsTer?
NM_018656.2:c.4dup	NP_061126.2:p.Ala2GlyfsTer?
XM_005269006.2:c.4dup	XP_005269063.1:p.Ala2GlyfsTer?
NM_001354997.1:c.4dup	NP_001341926.1:p.Ala2GlyfsTer?
NM_001354998.1:c.4dup	NP_001341927.1:p.Ala2GlyfsTer?
NM_018656.3:c.4dup	NP_061126.2:p.Ala2GlyfsTer?
NR_149143.1:n.296dup
NR_149144.1:n.296dup
NM_001354997.3:c.4dup	NP_001341926.1:p.Ala2GlyfsTer?
NM_001354998.2:c.4dup	NP_001341927.1:p.Ala2GlyfsTer?
NM_018656.5:c.4dup MANE Select	NP_061126.2:p.Ala2GlyfsTer?
NR_149143.3:n.206dup
NR_149144.3:n.206dup