Canonical Allele Identifier: CA1167985719
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061505A= , CM000663.2:g.55061505A= GRCh38
NC_000001.10:g.55527178A= , CM000663.1:g.55527178A= GRCh37
NC_000001.9:g.55299766A= NCBI36
NG_009061.1:g.26959A= , LRG_275:g.26959A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*152A= ENSP00000501161.2:n.*152A=
ENST00000710286.1:c.2169A= ENSP00000518176.1:p.Pro723=
ENST00000673903.1:c.1437A= ENSP00000501257.1:p.Pro479=
ENST00000673913.1:c.662A= ENSP00000501161.1:n.662A=
ENST00000302118.5:c.1812A= MANE Select ENSP00000303208.5:p.Pro604=
ENST00000490692.1:n.2358A=
NM_174936.3:c.1812A= , LRG_275t1:c.1812A= NP_777596.2:p.Pro604=
NR_110451.1:n.1419A=
XM_011541193.1:c.933A= XP_011539495.1:p.Pro311=
NM_174936.4:c.1812A= MANE Select NP_777596.2:p.Pro604=
NR_110451.2:n.1419A=