Canonical Allele Identifier: CA15305228
Gene: ELOVL6 HGNC NCBI

Linked Data

dbSNP Id: rs10011926

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110105771C>T , CM000666.2:g.110105771C>T GRCh38
NC_000004.11:g.111026927C>T , CM000666.1:g.111026927C>T GRCh37
NC_000004.10:g.111246376C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302274.8:c.90-143G>A MANE Select ENSP00000304736.3:p.=
ENST00000302274.7:c.90-143G>A ENSP00000304736.3:p.=
ENST00000394607.7:c.90-143G>A ENSP00000378105.3:p.=
ENST00000503885.1:c.90-143G>A ENSP00000426086.1:p.=
ENST00000506461.1:n.305-143G>A
ENST00000506625.5:c.90-143G>A ENSP00000425488.1:p.=
ENST00000514184.5:c.90-143G>A ENSP00000424023.1:p.=
NM_001130721.1:c.90-143G>A NP_001124193.1:p.=
NM_024090.2:c.90-143G>A NP_076995.1:p.=
XM_011532233.1:c.90-143G>A XP_011530535.1:p.=
XM_011532234.1:c.90-143G>A XP_011530536.1:p.=
XM_011532235.1:c.-192-143G>A XP_011530537.1:p.=
XM_011532233.3:c.90-143G>A XP_011530535.1:p.=
XM_011532234.3:c.90-143G>A XP_011530536.1:p.=
NM_001130721.2:c.90-143G>A NP_001124193.1:p.=
NM_024090.3:c.90-143G>A MANE Select NP_076995.1:p.=