Canonical Allele Identifier: CA6678235
Gene: SLC35E3 HGNC NCBI

Linked Data

dbSNP Id: rs774335982

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746385del , CM000674.2:g.68746385del GRCh38
NC_000012.11:g.69140165del , CM000674.1:g.69140165del GRCh37
NC_000012.10:g.67426432del NCBI36
NG_046600.2:g.64435del

Transcript Alleles

HGVS Amino-acid Change
ENST00000319429.7:n.251del
ENST00000398004.4:c.8del MANE Select ENSP00000381089.2:p.Leu3CysfsTer?
ENST00000673712.1:c.8del ENSP00000501065.1:p.Leu3CysfsTer?
ENST00000674096.1:c.8del ENSP00000501130.1:p.Leu3CysfsTer?
ENST00000398004.3:c.8del ENSP00000381089.2:p.Leu3CysfsTer?
NM_018656.2:c.8del NP_061126.2:p.Leu3CysfsTer?
XM_005269006.2:c.8del XP_005269063.1:p.Leu3CysfsTer?
NM_001354997.1:c.8del NP_001341926.1:p.Leu3CysfsTer?
NM_001354998.1:c.8del NP_001341927.1:p.Leu3CysfsTer?
NM_018656.3:c.8del NP_061126.2:p.Leu3CysfsTer?
NR_149143.1:n.300del
NR_149144.1:n.300del
NM_001354997.3:c.8del NP_001341926.1:p.Leu3CysfsTer?
NM_001354998.2:c.8del NP_001341927.1:p.Leu3CysfsTer?
NM_018656.5:c.8del MANE Select NP_061126.2:p.Leu3CysfsTer?
NR_149143.3:n.210del
NR_149144.3:n.210del