Canonical Allele Identifier: CA1167984869

Gene: PCSK9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059464_55059465delinsCA , CM000663.2:g.55059464_55059465delinsCA	GRCh38
NC_000001.10:g.55525137_55525138delinsCA , CM000663.1:g.55525137_55525138delinsCA	GRCh37
NC_000001.9:g.55297725_55297726delinsCA	NCBI36
NG_009061.1:g.24918_24919delinsCA , LRG_275:g.24918_24919delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1504-22_1504-21delinsCA	ENSP00000501161.2:n.1504-22_1504-21delinsCA
ENST00000710286.1:c.1861-22_1861-21delinsCA	ENSP00000518176.1:n.1861-22_1861-21delinsCA
ENST00000673903.1:c.1129-22_1129-21delinsCA	ENSP00000501257.1:n.1129-22_1129-21delinsCA
ENST00000673913.1:c.244-22_244-21delinsCA	ENSP00000501161.1:n.244-22_244-21delinsCA
ENST00000302118.5:c.1504-22_1504-21delinsCA MANE Select	ENSP00000303208.5:n.1504-22_1504-21delinsCA
ENST00000490692.1:n.2227+817_2227+818delinsCA
NM_174936.3:c.1504-22_1504-21delinsCA , LRG_275t1:c.1504-22_1504-21delinsCA	NP_777596.2:n.1504-22_1504-21delinsCA
NR_110451.1:n.1111-22_1111-21delinsCA
XM_011541193.1:c.625-22_625-21delinsCA	XP_011539495.1:n.625-22_625-21delinsCA
NM_174936.4:c.1504-22_1504-21delinsCA MANE Select	NP_777596.2:n.1504-22_1504-21delinsCA
NR_110451.2:n.1111-22_1111-21delinsCA