Canonical Allele Identifier: CA1484848612
Gene: ELOVL6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110105675A= , CM000666.2:g.110105675A= GRCh38
NC_000004.11:g.111026831A= , CM000666.1:g.111026831A= GRCh37
NC_000004.10:g.111246280A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302274.8:c.90-47T= MANE Select ENSP00000304736.3:n.90-47T=
ENST00000302274.7:c.90-47T= ENSP00000304736.3:n.90-47T=
ENST00000394607.7:c.90-47T= ENSP00000378105.3:n.90-47T=
ENST00000503885.1:c.90-47T= ENSP00000426086.1:n.90-47T=
ENST00000506461.1:n.305-47T=
ENST00000506625.5:c.90-47T= ENSP00000425488.1:n.90-47T=
ENST00000514184.5:c.90-47T= ENSP00000424023.1:n.90-47T=
NM_001130721.1:c.90-47T= NP_001124193.1:n.90-47T=
NM_024090.2:c.90-47T= NP_076995.1:n.90-47T=
XM_011532233.1:c.90-47T= XP_011530535.1:n.90-47T=
XM_011532234.1:c.90-47T= XP_011530536.1:n.90-47T=
XM_011532235.1:c.-192-47T= XP_011530537.1:n.-192-47T=
XM_011532233.3:c.90-47T= XP_011530535.1:n.90-47T=
XM_011532234.3:c.90-47T= XP_011530536.1:n.90-47T=
NM_001130721.2:c.90-47T= NP_001124193.1:n.90-47T=
NM_024090.3:c.90-47T= MANE Select NP_076995.1:n.90-47T=