Canonical Allele Identifier: CA385700280
Gene: SLC35E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746459A>T , CM000674.2:g.68746459A>T GRCh38
NC_000012.11:g.69140239A>T , CM000674.1:g.69140239A>T GRCh37
NC_000012.10:g.67426506A>T NCBI36
NG_046600.2:g.64509A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319429.7:n.325A>T
ENST00000398004.4:c.82A>T MANE Select ENSP00000381089.2:p.Ile28Phe
ENST00000673712.1:c.82A>T ENSP00000501065.1:p.Ile28Phe
ENST00000674096.1:c.82A>T ENSP00000501130.1:p.Ile28Phe
ENST00000398004.3:c.82A>T ENSP00000381089.2:p.Ile28Phe
NM_018656.2:c.82A>T NP_061126.2:p.Ile28Phe
XM_005269006.2:c.82A>T XP_005269063.1:p.Ile28Phe
NM_001354997.1:c.82A>T NP_001341926.1:p.Ile28Phe
NM_001354998.1:c.82A>T NP_001341927.1:p.Ile28Phe
NM_018656.3:c.82A>T NP_061126.2:p.Ile28Phe
NR_149143.1:n.374A>T
NR_149144.1:n.374A>T
NM_001354997.3:c.82A>T NP_001341926.1:p.Ile28Phe
NM_001354998.2:c.82A>T NP_001341927.1:p.Ile28Phe
NM_018656.5:c.82A>T MANE Select NP_061126.2:p.Ile28Phe
NR_149143.3:n.284A>T
NR_149144.3:n.284A>T