Canonical Allele Identifier: CA2044020466

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746827T= , CM000674.2:g.68746827T=	GRCh38
NC_000012.11:g.69140607T= , CM000674.1:g.69140607T=	GRCh37
NC_000012.10:g.67426874T=	NCBI36
NG_046600.2:g.64877T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.645+48T=
ENST00000398004.4:c.402+48T= MANE Select	ENSP00000381089.2:n.402+48T=
ENST00000673712.1:c.402+48T=	ENSP00000501065.1:n.402+48T=
ENST00000674096.1:c.402+48T=	ENSP00000501130.1:n.402+48T=
ENST00000398004.3:c.402+48T=	ENSP00000381089.2:n.402+48T=
NM_018656.2:c.402+48T=	NP_061126.2:n.402+48T=
XM_005269006.2:c.402+48T=	XP_005269063.1:n.402+48T=
NM_001354997.1:c.402+48T=	NP_001341926.1:n.402+48T=
NM_001354998.1:c.402+48T=	NP_001341927.1:n.402+48T=
NM_018656.3:c.402+48T=	NP_061126.2:n.402+48T=
NR_149143.1:n.694+48T=
NR_149144.1:n.694+48T=
NM_001354997.3:c.402+48T=	NP_001341926.1:n.402+48T=
NM_001354998.2:c.402+48T=	NP_001341927.1:n.402+48T=
NM_018656.5:c.402+48T= MANE Select	NP_061126.2:n.402+48T=
NR_149143.3:n.604+48T=
NR_149144.3:n.604+48T=