Canonical Allele Identifier: CA1167984839

Gene: PCSK9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059384_55059385delinsAG , CM000663.2:g.55059384_55059385delinsAG	GRCh38
NC_000001.10:g.55525057_55525058delinsAG , CM000663.1:g.55525057_55525058delinsAG	GRCh37
NC_000001.9:g.55297645_55297646delinsAG	NCBI36
NG_009061.1:g.24838_24839delinsAG , LRG_275:g.24838_24839delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000673913.2:c.1504-102_1504-101delinsAG	ENSP00000501161.2:n.1504-102_1504-101delinsAG
ENST00000710286.1:c.1861-102_1861-101delinsAG	ENSP00000518176.1:n.1861-102_1861-101delinsAG
ENST00000673903.1:c.1129-102_1129-101delinsAG	ENSP00000501257.1:n.1129-102_1129-101delinsAG
ENST00000673913.1:c.244-102_244-101delinsAG	ENSP00000501161.1:n.244-102_244-101delinsAG
ENST00000302118.5:c.1504-102_1504-101delinsAG MANE Select	ENSP00000303208.5:n.1504-102_1504-101delinsAG
ENST00000490692.1:n.2227+737_2227+738delinsAG
NM_174936.3:c.1504-102_1504-101delinsAG , LRG_275t1:c.1504-102_1504-101delinsAG	NP_777596.2:n.1504-102_1504-101delinsAG
NR_110451.1:n.1111-102_1111-101delinsAG
XM_011541193.1:c.625-102_625-101delinsAG	XP_011539495.1:n.625-102_625-101delinsAG
NM_174936.4:c.1504-102_1504-101delinsAG MANE Select	NP_777596.2:n.1504-102_1504-101delinsAG
NR_110451.2:n.1111-102_1111-101delinsAG