Canonical Allele Identifier: CA417960294

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55524233A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55058560A>T , CM000663.2:g.55058560A>T	GRCh38
NC_000001.10:g.55524233A>T , CM000663.1:g.55524233A>T	GRCh37
NC_000001.9:g.55296821A>T	NCBI36
NG_009061.1:g.24014A>T , LRG_275:g.24014A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1416A>T	ENSP00000501161.2:p.Thr472=
ENST00000710286.1:c.1773A>T	ENSP00000518176.1:p.Thr591=
ENST00000673903.1:c.1041A>T	ENSP00000501257.1:p.Thr347=
ENST00000673913.1:c.156A>T	ENSP00000501161.1:p.Thr52=
ENST00000302118.5:c.1416A>T MANE Select	ENSP00000303208.5:p.Thr472=
ENST00000490692.1:n.2140A>T
NM_174936.3:c.1416A>T , LRG_275t1:c.1416A>T	NP_777596.2:p.Thr472=
NR_110451.1:n.1023A>T
XM_011541193.1:c.537A>T	XP_011539495.1:p.Thr179=
NM_174936.4:c.1416A>T MANE Select	NP_777596.2:p.Thr472=
NR_110451.2:n.1023A>T