Canonical Allele Identifier: CA1167978122
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55043919C= , CM000663.2:g.55043919C= GRCh38
NC_000001.10:g.55509592C= , CM000663.1:g.55509592C= GRCh37
NC_000001.9:g.55282180C= NCBI36
NG_009061.1:g.9373C= , LRG_275:g.9373C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.284C= ENSP00000501161.2:p.Ala95=
ENST00000710286.1:c.641C= ENSP00000518176.1:p.Ala214=
ENST00000673726.1:c.284C= ENSP00000501004.1:p.Ala95=
ENST00000673903.1:c.-92C= ENSP00000501257.1:n.-92C=
ENST00000302118.5:c.284C= MANE Select ENSP00000303208.5:p.Ala95=
NM_174936.3:c.284C= , LRG_275t1:c.284C= NP_777596.2:p.Ala95=
NR_110451.1:n.182+3516C=
NM_174936.4:c.284C= MANE Select NP_777596.2:p.Ala95=
NR_110451.2:n.182+3516C=