Canonical Allele Identifier: CA1167986676

Gene: PCSK9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55063835_55063839delinsCCATT , CM000663.2:g.55063835_55063839delinsCCATT	GRCh38
NC_000001.10:g.55529508_55529512delinsCCATT , CM000663.1:g.55529508_55529512delinsCCATT	GRCh37
NC_000001.9:g.55302096_55302100delinsCCATT	NCBI36
NG_009061.1:g.29289_29293delinsCCATT , LRG_275:g.29289_29293delinsCCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*670_*674delinsCCATT	ENSP00000501161.2:n.*670_*674delinsCCATT
ENST00000710286.1:c.*251_*255delinsCCATT	ENSP00000518176.1:n.*251_*255delinsCCATT
ENST00000673903.1:c.*251_*255delinsCCATT	ENSP00000501257.1:n.*251_*255delinsCCATT
ENST00000302118.5:c.*251_*255delinsCCATT MANE Select	ENSP00000303208.5:n.*251_*255delinsCCATT
ENST00000490692.1:n.2876_2880delinsCCATT
NM_174936.3:c.*251_*255delinsCCATT , LRG_275t1:c.*251_*255delinsCCATT	NP_777596.2:n.*251_*255delinsCCATT
NR_110451.1:n.1937_1941delinsCCATT
XM_011541193.1:c.*251_*255delinsCCATT	XP_011539495.1:n.*251_*255delinsCCATT
NM_174936.4:c.*251_*255delinsCCATT MANE Select	NP_777596.2:n.*251_*255delinsCCATT
NR_110451.2:n.1937_1941delinsCCATT