Canonical Allele Identifier: CA340480434

Gene: PCSK9

Linked Data

• gnomAD v4: 1-55061512-G-T
• MyVariant Identifiers: chr1:g.55527185G>T (hg19) ; chr1:g.55061512G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55061512G>T , CM000663.2:g.55061512G>T	GRCh38
NC_000001.10:g.55527185G>T , CM000663.1:g.55527185G>T	GRCh37
NC_000001.9:g.55299773G>T	NCBI36
NG_009061.1:g.26966G>T , LRG_275:g.26966G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*159G>T	ENSP00000501161.2:n.*159G>T
ENST00000710286.1:c.2176G>T	ENSP00000518176.1:p.Glu726Ter
ENST00000673903.1:c.1444G>T	ENSP00000501257.1:p.Glu482Ter
ENST00000673913.1:c.669G>T	ENSP00000501161.1:n.669G>T
ENST00000302118.5:c.1819G>T MANE Select	ENSP00000303208.5:p.Glu607Ter
ENST00000490692.1:n.2365G>T
NM_174936.3:c.1819G>T , LRG_275t1:c.1819G>T	NP_777596.2:p.Glu607Ter
NR_110451.1:n.1426G>T
XM_011541193.1:c.940G>T	XP_011539495.1:p.Glu314Ter
NM_174936.4:c.1819G>T MANE Select	NP_777596.2:p.Glu607Ter
NR_110451.2:n.1426G>T