Canonical Allele Identifier: CA1167986497
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063420C= , CM000663.2:g.55063420C= GRCh38
NC_000001.10:g.55529093C= , CM000663.1:g.55529093C= GRCh37
NC_000001.9:g.55301681C= NCBI36
NG_009061.1:g.28874C= , LRG_275:g.28874C=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.*255C= ENSP00000501161.2:n.*255C=
ENST00000710286.1:c.2272C= ENSP00000518176.1:p.Pro758=
ENST00000673903.1:c.1540C= ENSP00000501257.1:p.Pro514=
ENST00000673913.1:c.765C= ENSP00000501161.1:n.765C=
ENST00000302118.5:c.1915C= MANE Select ENSP00000303208.5:p.Pro639=
ENST00000490692.1:n.2461C=
NM_174936.3:c.1915C= , LRG_275t1:c.1915C= NP_777596.2:p.Pro639=
NR_110451.1:n.1522C=
XM_011541193.1:c.1036C= XP_011539495.1:p.Pro346=
NM_174936.4:c.1915C= MANE Select NP_777596.2:p.Pro639=
NR_110451.2:n.1522C=