Canonical Allele Identifier: CA417957472

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55509539C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55043866C>G , CM000663.2:g.55043866C>G	GRCh38
NC_000001.10:g.55509539C>G , CM000663.1:g.55509539C>G	GRCh37
NC_000001.9:g.55282127C>G	NCBI36
NG_009061.1:g.9320C>G , LRG_275:g.9320C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.231C>G	ENSP00000501161.2:p.Thr77=
ENST00000710286.1:c.588C>G	ENSP00000518176.1:p.Thr196=
ENST00000673726.1:c.231C>G	ENSP00000501004.1:p.Thr77=
ENST00000673903.1:c.-145C>G	ENSP00000501257.1:n.-145C>G
ENST00000302118.5:c.231C>G MANE Select	ENSP00000303208.5:p.Thr77=
NM_174936.3:c.231C>G , LRG_275t1:c.231C>G	NP_777596.2:p.Thr77=
NR_110451.1:n.182+3463C>G
NM_174936.4:c.231C>G MANE Select	NP_777596.2:p.Thr77=
NR_110451.2:n.182+3463C>G