Canonical Allele Identifier: CA385700707
Gene: SLC35E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746660C>A , CM000674.2:g.68746660C>A GRCh38
NC_000012.11:g.69140440C>A , CM000674.1:g.69140440C>A GRCh37
NC_000012.10:g.67426707C>A NCBI36
NG_046600.2:g.64710C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319429.7:n.526C>A
ENST00000398004.4:c.283C>A MANE Select ENSP00000381089.2:p.Leu95Met
ENST00000673712.1:c.283C>A ENSP00000501065.1:p.Leu95Met
ENST00000674096.1:c.283C>A ENSP00000501130.1:p.Leu95Met
ENST00000398004.3:c.283C>A ENSP00000381089.2:p.Leu95Met
NM_018656.2:c.283C>A NP_061126.2:p.Leu95Met
XM_005269006.2:c.283C>A XP_005269063.1:p.Leu95Met
NM_001354997.1:c.283C>A NP_001341926.1:p.Leu95Met
NM_001354998.1:c.283C>A NP_001341927.1:p.Leu95Met
NM_018656.3:c.283C>A NP_061126.2:p.Leu95Met
NR_149143.1:n.575C>A
NR_149144.1:n.575C>A
NM_001354997.3:c.283C>A NP_001341926.1:p.Leu95Met
NM_001354998.2:c.283C>A NP_001341927.1:p.Leu95Met
NM_018656.5:c.283C>A MANE Select NP_061126.2:p.Leu95Met
NR_149143.3:n.485C>A
NR_149144.3:n.485C>A