Canonical Allele Identifier: CA357982667
Gene: ELOVL6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110105545T>A , CM000666.2:g.110105545T>A GRCh38
NC_000004.11:g.111026701T>A , CM000666.1:g.111026701T>A GRCh37
NC_000004.10:g.111246150T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302274.8:c.173A>T MANE Select ENSP00000304736.3:p.Glu58Val
ENST00000302274.7:c.173A>T ENSP00000304736.3:p.Glu58Val
ENST00000394607.7:c.173A>T ENSP00000378105.3:p.Glu58Val
ENST00000503885.1:c.173A>T ENSP00000426086.1:p.Glu58Val
ENST00000506461.1:n.388A>T
ENST00000506625.5:c.173A>T ENSP00000425488.1:p.Glu58Val
ENST00000514184.5:c.173A>T ENSP00000424023.1:p.Glu58Val
NM_001130721.1:c.173A>T NP_001124193.1:p.Glu58Val
NM_024090.2:c.173A>T NP_076995.1:p.Glu58Val
XM_011532233.1:c.173A>T XP_011530535.1:p.Glu58Val
XM_011532234.1:c.173A>T XP_011530536.1:p.Glu58Val
XM_011532235.1:c.-109A>T XP_011530537.1:n.-109A>T
XM_011532233.3:c.173A>T XP_011530535.1:p.Glu58Val
XM_011532234.3:c.173A>T XP_011530536.1:p.Glu58Val
NM_001130721.2:c.173A>T NP_001124193.1:p.Glu58Val
NM_024090.3:c.173A>T MANE Select NP_076995.1:p.Glu58Val