Canonical Allele Identifier: CA417957568

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55509671C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55043998C>G , CM000663.2:g.55043998C>G	GRCh38
NC_000001.10:g.55509671C>G , CM000663.1:g.55509671C>G	GRCh37
NC_000001.9:g.55282259C>G	NCBI36
NG_009061.1:g.9452C>G , LRG_275:g.9452C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.363C>G	ENSP00000501161.2:p.Gly121=
ENST00000710286.1:c.720C>G	ENSP00000518176.1:p.Gly240=
ENST00000673662.1:n.33C>G
ENST00000673726.1:c.363C>G	ENSP00000501004.1:p.Gly121=
ENST00000673903.1:c.-13C>G	ENSP00000501257.1:n.-13C>G
ENST00000302118.5:c.363C>G MANE Select	ENSP00000303208.5:p.Gly121=
NM_174936.3:c.363C>G , LRG_275t1:c.363C>G	NP_777596.2:p.Gly121=
NR_110451.1:n.182+3595C>G
NM_174936.4:c.363C>G MANE Select	NP_777596.2:p.Gly121=
NR_110451.2:n.182+3595C>G