Canonical Allele Identifier: CA340479892

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55525231T>A (hg19) ; chr1:g.55059558T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059558T>A , CM000663.2:g.55059558T>A	GRCh38
NC_000001.10:g.55525231T>A , CM000663.1:g.55525231T>A	GRCh37
NC_000001.9:g.55297819T>A	NCBI36
NG_009061.1:g.25012T>A , LRG_275:g.25012T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1576T>A	ENSP00000501161.2:p.Cys526Ser
ENST00000710286.1:c.1933T>A	ENSP00000518176.1:p.Cys645Ser
ENST00000673903.1:c.1201T>A	ENSP00000501257.1:p.Cys401Ser
ENST00000673913.1:c.316T>A	ENSP00000501161.1:p.Cys106Ser
ENST00000302118.5:c.1576T>A MANE Select	ENSP00000303208.5:p.Cys526Ser
ENST00000490692.1:n.2227+911T>A
NM_174936.3:c.1576T>A , LRG_275t1:c.1576T>A	NP_777596.2:p.Cys526Ser
NR_110451.1:n.1183T>A
XM_011541193.1:c.697T>A	XP_011539495.1:p.Cys233Ser
NM_174936.4:c.1576T>A MANE Select	NP_777596.2:p.Cys526Ser
NR_110451.2:n.1183T>A