Canonical Allele Identifier: CA1066632647
Gene: ELOVL6 HGNC NCBI

Linked Data

dbSNP Id: rs1756868222

Genomic Alleles

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

Transcript Alleles

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