Canonical Allele Identifier: CA1167986585
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063628G= , CM000663.2:g.55063628G= GRCh38
NC_000001.10:g.55529301G= , CM000663.1:g.55529301G= GRCh37
NC_000001.9:g.55301889G= NCBI36
NG_009061.1:g.29082G= , LRG_275:g.29082G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*463G= ENSP00000501161.2:n.*463G=
ENST00000710286.1:c.*44G= ENSP00000518176.1:n.*44G=
ENST00000673903.1:c.*44G= ENSP00000501257.1:n.*44G=
ENST00000302118.5:c.*44G= MANE Select ENSP00000303208.5:n.*44G=
ENST00000490692.1:n.2669G=
NM_174936.3:c.*44G= , LRG_275t1:c.*44G= NP_777596.2:n.*44G=
NR_110451.1:n.1730G=
XM_011541193.1:c.*44G= XP_011539495.1:n.*44G=
NM_174936.4:c.*44G= MANE Select NP_777596.2:n.*44G=
NR_110451.2:n.1730G=