Canonical Allele Identifier: CA2796414562

Gene: SLC35E3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746370_68746373del , CM000674.2:g.68746370_68746373del	GRCh38
NC_000012.11:g.69140150_69140153del , CM000674.1:g.69140150_69140153del	GRCh37
NC_000012.10:g.67426417_67426420del	NCBI36
NG_046600.2:g.64420_64423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.236_239del
ENST00000398004.4:c.-8_-5del MANE Select	ENSP00000381089.2:n.-8_-5del
ENST00000673712.1:c.-8_-5del	ENSP00000501065.1:n.-8_-5del
ENST00000674096.1:c.-8_-5del	ENSP00000501130.1:n.-8_-5del
ENST00000398004.3:c.-8_-5del	ENSP00000381089.2:n.-8_-5del
NM_018656.2:c.-8_-5del	NP_061126.2:n.-8_-5del
XM_005269006.2:c.-8_-5del	XP_005269063.1:n.-8_-5del
NM_001354997.1:c.-8_-5del	NP_001341926.1:n.-8_-5del
NM_001354998.1:c.-8_-5del	NP_001341927.1:n.-8_-5del
NM_018656.3:c.-8_-5del	NP_061126.2:n.-8_-5del
NR_149143.1:n.285_288del
NR_149144.1:n.285_288del
NM_001354997.3:c.-8_-5del	NP_001341926.1:n.-8_-5del
NM_001354998.2:c.-8_-5del	NP_001341927.1:n.-8_-5del
NM_018656.5:c.-8_-5del MANE Select	NP_061126.2:n.-8_-5del
NR_149143.3:n.195_198del
NR_149144.3:n.195_198del