Canonical Allele Identifier: CA1167986646
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063761A= , CM000663.2:g.55063761A= GRCh38
NC_000001.10:g.55529434A= , CM000663.1:g.55529434A= GRCh37
NC_000001.9:g.55302022A= NCBI36
NG_009061.1:g.29215A= , LRG_275:g.29215A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*596A= ENSP00000501161.2:n.*596A=
ENST00000710286.1:c.*177A= ENSP00000518176.1:n.*177A=
ENST00000673903.1:c.*177A= ENSP00000501257.1:n.*177A=
ENST00000302118.5:c.*177A= MANE Select ENSP00000303208.5:n.*177A=
ENST00000490692.1:n.2802A=
NM_174936.3:c.*177A= , LRG_275t1:c.*177A= NP_777596.2:n.*177A=
NR_110451.1:n.1863A=
XM_011541193.1:c.*177A= XP_011539495.1:n.*177A=
NM_174936.4:c.*177A= MANE Select NP_777596.2:n.*177A=
NR_110451.2:n.1863A=