Canonical Allele Identifier: CA645813901

Gene: PCSK9

Linked Data

• dbSNP Id: rs1644741389
• COSMIC: COSN1449414

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059334C>T , CM000663.2:g.55059334C>T	GRCh38
NC_000001.10:g.55525007C>T , CM000663.1:g.55525007C>T	GRCh37
NC_000001.9:g.55297595C>T	NCBI36
NG_009061.1:g.24788C>T , LRG_275:g.24788C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000673913.2:c.1504-152C>T	ENSP00000501161.2:n.1504-152C>T
ENST00000710286.1:c.1861-152C>T	ENSP00000518176.1:n.1861-152C>T
ENST00000673903.1:c.1129-152C>T	ENSP00000501257.1:n.1129-152C>T
ENST00000673913.1:c.244-152C>T	ENSP00000501161.1:n.244-152C>T
ENST00000302118.5:c.1504-152C>T MANE Select	ENSP00000303208.5:n.1504-152C>T
ENST00000490692.1:n.2227+687C>T
NM_174936.3:c.1504-152C>T , LRG_275t1:c.1504-152C>T	NP_777596.2:n.1504-152C>T
NR_110451.1:n.1111-152C>T
XM_011541193.1:c.625-152C>T	XP_011539495.1:n.625-152C>T
NM_174936.4:c.1504-152C>T MANE Select	NP_777596.2:n.1504-152C>T
NR_110451.2:n.1111-152C>T