Canonical Allele Identifier: CA1167985007

Gene: PCSK9

Linked Data

• dbSNP Id: rs1644745878

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059785_55059786insGC , CM000663.2:g.55059785_55059786insGC	GRCh38
NC_000001.10:g.55525458_55525459insGC , CM000663.1:g.55525458_55525459insGC	GRCh37
NC_000001.9:g.55298046_55298047insGC	NCBI36
NG_009061.1:g.25239_25240insGC , LRG_275:g.25239_25240insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1681+122_1681+123insGC	ENSP00000501161.2:n.1681+122_1681+123insGC
ENST00000710286.1:c.2038+122_2038+123insGC	ENSP00000518176.1:n.2038+122_2038+123insGC
ENST00000673903.1:c.1306+122_1306+123insGC	ENSP00000501257.1:n.1306+122_1306+123insGC
ENST00000673913.1:c.421+122_421+123insGC	ENSP00000501161.1:n.421+122_421+123insGC
ENST00000302118.5:c.1681+122_1681+123insGC MANE Select	ENSP00000303208.5:n.1681+122_1681+123insGC
ENST00000490692.1:n.2227+1138_2227+1139insGC
NM_174936.3:c.1681+122_1681+123insGC , LRG_275t1:c.1681+122_1681+123insGC	NP_777596.2:n.1681+122_1681+123insGC
NR_110451.1:n.1288+122_1288+123insGC
XM_011541193.1:c.802+122_802+123insGC	XP_011539495.1:n.802+122_802+123insGC
NM_174936.4:c.1681+122_1681+123insGC MANE Select	NP_777596.2:n.1681+122_1681+123insGC
NR_110451.2:n.1288+122_1288+123insGC