Canonical Allele Identifier: CA1167986626
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063708C= , CM000663.2:g.55063708C= GRCh38
NC_000001.10:g.55529381C= , CM000663.1:g.55529381C= GRCh37
NC_000001.9:g.55301969C= NCBI36
NG_009061.1:g.29162C= , LRG_275:g.29162C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*543C= ENSP00000501161.2:n.*543C=
ENST00000710286.1:c.*124C= ENSP00000518176.1:n.*124C=
ENST00000673903.1:c.*124C= ENSP00000501257.1:n.*124C=
ENST00000302118.5:c.*124C= MANE Select ENSP00000303208.5:n.*124C=
ENST00000490692.1:n.2749C=
NM_174936.3:c.*124C= , LRG_275t1:c.*124C= NP_777596.2:n.*124C=
NR_110451.1:n.1810C=
XM_011541193.1:c.*124C= XP_011539495.1:n.*124C=
NM_174936.4:c.*124C= MANE Select NP_777596.2:n.*124C=
NR_110451.2:n.1810C=