Canonical Allele Identifier: CA1167986667
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063809T= , CM000663.2:g.55063809T= GRCh38
NC_000001.10:g.55529482T= , CM000663.1:g.55529482T= GRCh37
NC_000001.9:g.55302070T= NCBI36
NG_009061.1:g.29263T= , LRG_275:g.29263T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*644T= ENSP00000501161.2:n.*644T=
ENST00000710286.1:c.*225T= ENSP00000518176.1:n.*225T=
ENST00000673903.1:c.*225T= ENSP00000501257.1:n.*225T=
ENST00000302118.5:c.*225T= MANE Select ENSP00000303208.5:n.*225T=
ENST00000490692.1:n.2850T=
NM_174936.3:c.*225T= , LRG_275t1:c.*225T= NP_777596.2:n.*225T=
NR_110451.1:n.1911T=
XM_011541193.1:c.*225T= XP_011539495.1:n.*225T=
NM_174936.4:c.*225T= MANE Select NP_777596.2:n.*225T=
NR_110451.2:n.1911T=