Canonical Allele Identifier: CA417957586

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55509701G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55044028G>T , CM000663.2:g.55044028G>T	GRCh38
NC_000001.10:g.55509701G>T , CM000663.1:g.55509701G>T	GRCh37
NC_000001.9:g.55282289G>T	NCBI36
NG_009061.1:g.9482G>T , LRG_275:g.9482G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.393G>T	ENSP00000501161.2:p.Leu131=
ENST00000710286.1:c.750G>T	ENSP00000518176.1:p.Leu250=
ENST00000673662.1:n.63G>T
ENST00000673726.1:c.393G>T	ENSP00000501004.1:p.Leu131=
ENST00000673903.1:c.18G>T	ENSP00000501257.1:p.Leu6=
ENST00000302118.5:c.393G>T MANE Select	ENSP00000303208.5:p.Leu131=
NM_174936.3:c.393G>T , LRG_275t1:c.393G>T	NP_777596.2:p.Leu131=
NR_110451.1:n.182+3625G>T
NM_174936.4:c.393G>T MANE Select	NP_777596.2:p.Leu131=
NR_110451.2:n.182+3625G>T