Canonical Allele Identifier: CA2044020244

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746733_68746736delinsCCTT , CM000674.2:g.68746733_68746736delinsCCTT	GRCh38
NC_000012.11:g.69140513_69140516delinsCCTT , CM000674.1:g.69140513_69140516delinsCCTT	GRCh37
NC_000012.10:g.67426780_67426783delinsCCTT	NCBI36
NG_046600.2:g.64783_64786delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.599_602delinsCCTT
ENST00000398004.4:c.356_359delinsCCTT MANE Select	ENSP00000381089.2:p.Thr119=
ENST00000673712.1:c.356_359delinsCCTT	ENSP00000501065.1:p.Thr119=
ENST00000674096.1:c.356_359delinsCCTT	ENSP00000501130.1:p.Thr119=
ENST00000398004.3:c.356_359delinsCCTT	ENSP00000381089.2:p.Thr119=
NM_018656.2:c.356_359delinsCCTT	NP_061126.2:p.Thr119=
XM_005269006.2:c.356_359delinsCCTT	XP_005269063.1:p.Thr119=
NM_001354997.1:c.356_359delinsCCTT	NP_001341926.1:p.Thr119=
NM_001354998.1:c.356_359delinsCCTT	NP_001341927.1:p.Thr119=
NM_018656.3:c.356_359delinsCCTT	NP_061126.2:p.Thr119=
NR_149143.1:n.648_651delinsCCTT
NR_149144.1:n.648_651delinsCCTT
NM_001354997.3:c.356_359delinsCCTT	NP_001341926.1:p.Thr119=
NM_001354998.2:c.356_359delinsCCTT	NP_001341927.1:p.Thr119=
NM_018656.5:c.356_359delinsCCTT MANE Select	NP_061126.2:p.Thr119=
NR_149143.3:n.558_561delinsCCTT
NR_149144.3:n.558_561delinsCCTT