Canonical Allele Identifier: CA340480642

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55529088C>G (hg19) ; chr1:g.55063415C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55063415C>G , CM000663.2:g.55063415C>G	GRCh38
NC_000001.10:g.55529088C>G , CM000663.1:g.55529088C>G	GRCh37
NC_000001.9:g.55301676C>G	NCBI36
NG_009061.1:g.28869C>G , LRG_275:g.28869C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000673913.2:c.*250C>G	ENSP00000501161.2:n.*250C>G
ENST00000710286.1:c.2267C>G	ENSP00000518176.1:p.Ala756Gly
ENST00000673903.1:c.1535C>G	ENSP00000501257.1:p.Ala512Gly
ENST00000673913.1:c.760C>G	ENSP00000501161.1:n.760C>G
ENST00000302118.5:c.1910C>G MANE Select	ENSP00000303208.5:p.Ala637Gly
ENST00000490692.1:n.2456C>G
NM_174936.3:c.1910C>G , LRG_275t1:c.1910C>G	NP_777596.2:p.Ala637Gly
NR_110451.1:n.1517C>G
XM_011541193.1:c.1031C>G	XP_011539495.1:p.Ala344Gly
NM_174936.4:c.1910C>G MANE Select	NP_777596.2:p.Ala637Gly
NR_110451.2:n.1517C>G