Canonical Allele Identifier: CA606183519
Gene: SLC35E3 HGNC NCBI

Linked Data

dbSNP Id: rs1416115715

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746575_68746576del , CM000674.2:g.68746575_68746576del GRCh38
NC_000012.11:g.69140355_69140356del , CM000674.1:g.69140355_69140356del GRCh37
NC_000012.10:g.67426622_67426623del NCBI36
NG_046600.2:g.64625_64626del

Transcript Alleles

HGVS Amino-acid Change
ENST00000319429.7:n.441_442del
ENST00000398004.4:c.198_199del MANE Select ENSP00000381089.2:p.Phe67CysfsTer25
ENST00000673712.1:c.198_199del ENSP00000501065.1:p.Phe67CysfsTer25
ENST00000674096.1:c.198_199del ENSP00000501130.1:p.Phe67CysfsTer25
ENST00000398004.3:c.198_199del ENSP00000381089.2:p.Phe67CysfsTer25
NM_018656.2:c.198_199del NP_061126.2:p.Phe67CysfsTer25
XM_005269006.2:c.198_199del XP_005269063.1:p.Phe67CysfsTer25
NM_001354997.1:c.198_199del NP_001341926.1:p.Phe67CysfsTer25
NM_001354998.1:c.198_199del NP_001341927.1:p.Phe67CysfsTer25
NM_018656.3:c.198_199del NP_061126.2:p.Phe67CysfsTer25
NR_149143.1:n.490_491del
NR_149144.1:n.490_491del
NM_001354997.3:c.198_199del NP_001341926.1:p.Phe67CysfsTer25
NM_001354998.2:c.198_199del NP_001341927.1:p.Phe67CysfsTer25
NM_018656.5:c.198_199del MANE Select NP_061126.2:p.Phe67CysfsTer25
NR_149143.3:n.400_401del
NR_149144.3:n.400_401del