Canonical Allele Identifier: CA1167986602
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063662C= , CM000663.2:g.55063662C= GRCh38
NC_000001.10:g.55529335C= , CM000663.1:g.55529335C= GRCh37
NC_000001.9:g.55301923C= NCBI36
NG_009061.1:g.29116C= , LRG_275:g.29116C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*497C= ENSP00000501161.2:n.*497C=
ENST00000710286.1:c.*78C= ENSP00000518176.1:n.*78C=
ENST00000673903.1:c.*78C= ENSP00000501257.1:n.*78C=
ENST00000302118.5:c.*78C= MANE Select ENSP00000303208.5:n.*78C=
ENST00000490692.1:n.2703C=
NM_174936.3:c.*78C= , LRG_275t1:c.*78C= NP_777596.2:n.*78C=
NR_110451.1:n.1764C=
XM_011541193.1:c.*78C= XP_011539495.1:n.*78C=
NM_174936.4:c.*78C= MANE Select NP_777596.2:n.*78C=
NR_110451.2:n.1764C=