Canonical Allele Identifier: CA2044020516

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746862_68746864delinsCTT , CM000674.2:g.68746862_68746864delinsCTT	GRCh38
NC_000012.11:g.69140642_69140644delinsCTT , CM000674.1:g.69140642_69140644delinsCTT	GRCh37
NC_000012.10:g.67426909_67426911delinsCTT	NCBI36
NG_046600.2:g.64912_64914delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.645+83_645+85delinsCTT
ENST00000398004.4:c.402+83_402+85delinsCTT MANE Select	ENSP00000381089.2:n.402+83_402+85delinsCTT
ENST00000673712.1:c.402+83_402+85delinsCTT	ENSP00000501065.1:n.402+83_402+85delinsCTT
ENST00000674096.1:c.402+83_402+85delinsCTT	ENSP00000501130.1:n.402+83_402+85delinsCTT
ENST00000398004.3:c.402+83_402+85delinsCTT	ENSP00000381089.2:n.402+83_402+85delinsCTT
NM_018656.2:c.402+83_402+85delinsCTT	NP_061126.2:n.402+83_402+85delinsCTT
XM_005269006.2:c.402+83_402+85delinsCTT	XP_005269063.1:n.402+83_402+85delinsCTT
NM_001354997.1:c.402+83_402+85delinsCTT	NP_001341926.1:n.402+83_402+85delinsCTT
NM_001354998.1:c.402+83_402+85delinsCTT	NP_001341927.1:n.402+83_402+85delinsCTT
NM_018656.3:c.402+83_402+85delinsCTT	NP_061126.2:n.402+83_402+85delinsCTT
NR_149143.1:n.694+83_694+85delinsCTT
NR_149144.1:n.694+83_694+85delinsCTT
NM_001354997.3:c.402+83_402+85delinsCTT	NP_001341926.1:n.402+83_402+85delinsCTT
NM_001354998.2:c.402+83_402+85delinsCTT	NP_001341927.1:n.402+83_402+85delinsCTT
NM_018656.5:c.402+83_402+85delinsCTT MANE Select	NP_061126.2:n.402+83_402+85delinsCTT
NR_149143.3:n.604+83_604+85delinsCTT
NR_149144.3:n.604+83_604+85delinsCTT