Canonical Allele Identifier: CA1167986678
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063842A= , CM000663.2:g.55063842A= GRCh38
NC_000001.10:g.55529515A= , CM000663.1:g.55529515A= GRCh37
NC_000001.9:g.55302103A= NCBI36
NG_009061.1:g.29296A= , LRG_275:g.29296A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*677A= ENSP00000501161.2:n.*677A=
ENST00000710286.1:c.*258A= ENSP00000518176.1:n.*258A=
ENST00000673903.1:c.*258A= ENSP00000501257.1:n.*258A=
ENST00000302118.5:c.*258A= MANE Select ENSP00000303208.5:n.*258A=
ENST00000490692.1:n.2883A=
NM_174936.3:c.*258A= , LRG_275t1:c.*258A= NP_777596.2:n.*258A=
NR_110451.1:n.1944A=
XM_011541193.1:c.*258A= XP_011539495.1:n.*258A=
NM_174936.4:c.*258A= MANE Select NP_777596.2:n.*258A=
NR_110451.2:n.1944A=