Canonical Allele Identifier: CA1484848466

Gene: ELOVL6

Linked Data

• dbSNP Id: rs1756853591

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110105259_110105260insATCAAACAGATGACAACAGATCAAACA , CM000666.2:g.110105259_110105260insATCAAACAGATGACAACAGATCAAACA	GRCh38
NC_000004.11:g.111026415_111026416insATCAAACAGATGACAACAGATCAAACA , CM000666.1:g.111026415_111026416insATCAAACAGATGACAACAGATCAAACA	GRCh37
NC_000004.10:g.111245864_111245865insATCAAACAGATGACAACAGATCAAACA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302274.8:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT MANE Select	ENSP00000304736.3:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTT...
ENST00000302274.7:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	ENSP00000304736.3:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTT...
ENST00000394607.7:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	ENSP00000378105.3:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTT...
ENST00000503885.1:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	ENSP00000426086.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTT...
ENST00000506461.1:n.436+237_436+238insTGTTTGATCTGTTGTCATCTGTTTGAT
ENST00000506625.5:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	ENSP00000425488.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTT...
ENST00000514184.5:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	ENSP00000424023.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTT...
NM_001130721.1:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	NP_001124193.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGA...
NM_024090.2:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	NP_076995.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT
XM_011532233.1:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	XP_011530535.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGA...
XM_011532234.1:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	XP_011530536.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGA...
XM_011532235.1:c.-61+237_-61+238insTGTTTGATCTGTTGTCATCTGTTTGAT	XP_011530537.1:n.-61+237_-61+238insTGTTTGATCTGTTGTCATCTGTTTGA...
XM_011532233.3:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	XP_011530535.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGA...
XM_011532234.3:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	XP_011530536.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGA...
NM_001130721.2:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT	NP_001124193.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGA...
NM_024090.3:c.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT MANE Select	NP_076995.1:n.221+237_221+238insTGTTTGATCTGTTGTCATCTGTTTGAT