Canonical Allele Identifier: CA2044020090

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746652A= , CM000674.2:g.68746652A=	GRCh38
NC_000012.11:g.69140432A= , CM000674.1:g.69140432A=	GRCh37
NC_000012.10:g.67426699A=	NCBI36
NG_046600.2:g.64702A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.518A=
ENST00000398004.4:c.275A= MANE Select	ENSP00000381089.2:p.Asn92=
ENST00000673712.1:c.275A=	ENSP00000501065.1:p.Asn92=
ENST00000674096.1:c.275A=	ENSP00000501130.1:p.Asn92=
ENST00000398004.3:c.275A=	ENSP00000381089.2:p.Asn92=
NM_018656.2:c.275A=	NP_061126.2:p.Asn92=
XM_005269006.2:c.275A=	XP_005269063.1:p.Asn92=
NM_001354997.1:c.275A=	NP_001341926.1:p.Asn92=
NM_001354998.1:c.275A=	NP_001341927.1:p.Asn92=
NM_018656.3:c.275A=	NP_061126.2:p.Asn92=
NR_149143.1:n.567A=
NR_149144.1:n.567A=
NM_001354997.3:c.275A=	NP_001341926.1:p.Asn92=
NM_001354998.2:c.275A=	NP_001341927.1:p.Asn92=
NM_018656.5:c.275A= MANE Select	NP_061126.2:p.Asn92=
NR_149143.3:n.477A=
NR_149144.3:n.477A=