Canonical Allele Identifier: CA385700521
Gene: SLC35E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746571A>C , CM000674.2:g.68746571A>C GRCh38
NC_000012.11:g.69140351A>C , CM000674.1:g.69140351A>C GRCh37
NC_000012.10:g.67426618A>C NCBI36
NG_046600.2:g.64621A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319429.7:n.437A>C
ENST00000398004.4:c.194A>C MANE Select ENSP00000381089.2:p.Asp65Ala
ENST00000673712.1:c.194A>C ENSP00000501065.1:p.Asp65Ala
ENST00000674096.1:c.194A>C ENSP00000501130.1:p.Asp65Ala
ENST00000398004.3:c.194A>C ENSP00000381089.2:p.Asp65Ala
NM_018656.2:c.194A>C NP_061126.2:p.Asp65Ala
XM_005269006.2:c.194A>C XP_005269063.1:p.Asp65Ala
NM_001354997.1:c.194A>C NP_001341926.1:p.Asp65Ala
NM_001354998.1:c.194A>C NP_001341927.1:p.Asp65Ala
NM_018656.3:c.194A>C NP_061126.2:p.Asp65Ala
NR_149143.1:n.486A>C
NR_149144.1:n.486A>C
NM_001354997.3:c.194A>C NP_001341926.1:p.Asp65Ala
NM_001354998.2:c.194A>C NP_001341927.1:p.Asp65Ala
NM_018656.5:c.194A>C MANE Select NP_061126.2:p.Asp65Ala
NR_149143.3:n.396A>C
NR_149144.3:n.396A>C