Canonical Allele Identifier: CA417960542

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55527154C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55061481C>T , CM000663.2:g.55061481C>T	GRCh38
NC_000001.10:g.55527154C>T , CM000663.1:g.55527154C>T	GRCh37
NC_000001.9:g.55299742C>T	NCBI36
NG_009061.1:g.26935C>T , LRG_275:g.26935C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*128C>T	ENSP00000501161.2:n.*128C>T
ENST00000710286.1:c.2145C>T	ENSP00000518176.1:p.Ile715=
ENST00000673903.1:c.1413C>T	ENSP00000501257.1:p.Ile471=
ENST00000673913.1:c.638C>T	ENSP00000501161.1:n.638C>T
ENST00000302118.5:c.1788C>T MANE Select	ENSP00000303208.5:p.Ile596=
ENST00000490692.1:n.2334C>T
NM_174936.3:c.1788C>T , LRG_275t1:c.1788C>T	NP_777596.2:p.Ile596=
NR_110451.1:n.1395C>T
XM_011541193.1:c.909C>T	XP_011539495.1:p.Ile303=
NM_174936.4:c.1788C>T MANE Select	NP_777596.2:p.Ile596=
NR_110451.2:n.1395C>T