Canonical Allele Identifier: CA417960692

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55529200C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55063527C>G , CM000663.2:g.55063527C>G	GRCh38
NC_000001.10:g.55529200C>G , CM000663.1:g.55529200C>G	GRCh37
NC_000001.9:g.55301788C>G	NCBI36
NG_009061.1:g.28981C>G , LRG_275:g.28981C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*362C>G	ENSP00000501161.2:n.*362C>G
ENST00000710286.1:c.2379C>G	ENSP00000518176.1:p.Ala793=
ENST00000673903.1:c.1647C>G	ENSP00000501257.1:p.Ala549=
ENST00000673913.1:c.872C>G	ENSP00000501161.1:n.872C>G
ENST00000302118.5:c.2022C>G MANE Select	ENSP00000303208.5:p.Ala674=
ENST00000490692.1:n.2568C>G
NM_174936.3:c.2022C>G , LRG_275t1:c.2022C>G	NP_777596.2:p.Ala674=
NR_110451.1:n.1629C>G
XM_011541193.1:c.1143C>G	XP_011539495.1:p.Ala381=
NM_174936.4:c.2022C>G MANE Select	NP_777596.2:p.Ala674=
NR_110451.2:n.1629C>G