Canonical Allele Identifier: CA2671759223
Gene: ELOVL6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110105722del , CM000666.2:g.110105722del GRCh38
NC_000004.11:g.111026878del , CM000666.1:g.111026878del GRCh37
NC_000004.10:g.111246327del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302274.8:c.90-89del MANE Select ENSP00000304736.3:n.90-89del
ENST00000302274.7:c.90-89del ENSP00000304736.3:n.90-89del
ENST00000394607.7:c.90-89del ENSP00000378105.3:n.90-89del
ENST00000503885.1:c.90-89del ENSP00000426086.1:n.90-89del
ENST00000506461.1:n.305-89del
ENST00000506625.5:c.90-89del ENSP00000425488.1:n.90-89del
ENST00000514184.5:c.90-89del ENSP00000424023.1:n.90-89del
NM_001130721.1:c.90-89del NP_001124193.1:n.90-89del
NM_024090.2:c.90-89del NP_076995.1:n.90-89del
XM_011532233.1:c.90-89del XP_011530535.1:n.90-89del
XM_011532234.1:c.90-89del XP_011530536.1:n.90-89del
XM_011532235.1:c.-192-89del XP_011530537.1:n.-192-89del
XM_011532233.3:c.90-89del XP_011530535.1:n.90-89del
XM_011532234.3:c.90-89del XP_011530536.1:n.90-89del
NM_001130721.2:c.90-89del NP_001124193.1:n.90-89del
NM_024090.3:c.90-89del MANE Select NP_076995.1:n.90-89del