Canonical Allele Identifier: CA1167986590
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063641A= , CM000663.2:g.55063641A= GRCh38
NC_000001.10:g.55529314A= , CM000663.1:g.55529314A= GRCh37
NC_000001.9:g.55301902A= NCBI36
NG_009061.1:g.29095A= , LRG_275:g.29095A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*476A= ENSP00000501161.2:n.*476A=
ENST00000710286.1:c.*57A= ENSP00000518176.1:n.*57A=
ENST00000673903.1:c.*57A= ENSP00000501257.1:n.*57A=
ENST00000302118.5:c.*57A= MANE Select ENSP00000303208.5:n.*57A=
ENST00000490692.1:n.2682A=
NM_174936.3:c.*57A= , LRG_275t1:c.*57A= NP_777596.2:n.*57A=
NR_110451.1:n.1743A=
XM_011541193.1:c.*57A= XP_011539495.1:n.*57A=
NM_174936.4:c.*57A= MANE Select NP_777596.2:n.*57A=
NR_110451.2:n.1743A=