Canonical Allele Identifier: CA6678302
Gene: SLC35E3 HGNC NCBI

Linked Data

dbSNP Id: rs764011333

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746766del , CM000674.2:g.68746766del GRCh38
NC_000012.11:g.69140546del , CM000674.1:g.69140546del GRCh37
NC_000012.10:g.67426813del NCBI36
NG_046600.2:g.64816del

Transcript Alleles

HGVS Amino-acid Change
ENST00000319429.7:n.632del
ENST00000398004.4:c.389del MANE Select ENSP00000381089.2:p.Ile130ThrfsTer5
ENST00000673712.1:c.389del ENSP00000501065.1:p.Ile130ThrfsTer5
ENST00000674096.1:c.389del ENSP00000501130.1:p.Ile130ThrfsTer11
ENST00000398004.3:c.389del ENSP00000381089.2:p.Ile130ThrfsTer5
NM_018656.2:c.389del NP_061126.2:p.Ile130ThrfsTer5
XM_005269006.2:c.389del XP_005269063.1:p.Ile130ThrfsTer5
NM_001354997.1:c.389del NP_001341926.1:p.Ile130ThrfsTer7
NM_001354998.1:c.389del NP_001341927.1:p.Ile130ThrfsTer5
NM_018656.3:c.389del NP_061126.2:p.Ile130ThrfsTer5
NR_149143.1:n.681del
NR_149144.1:n.681del
NM_001354997.3:c.389del NP_001341926.1:p.Ile130ThrfsTer7
NM_001354998.2:c.389del NP_001341927.1:p.Ile130ThrfsTer5
NM_018656.5:c.389del MANE Select NP_061126.2:p.Ile130ThrfsTer5
NR_149143.3:n.591del
NR_149144.3:n.591del