Canonical Allele Identifier: CA2645841848

Gene: PCSK9

Linked Data

• gnomAD v4: 1-55059815-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059815G>A , CM000663.2:g.55059815G>A	GRCh38
NC_000001.10:g.55525488G>A , CM000663.1:g.55525488G>A	GRCh37
NC_000001.9:g.55298076G>A	NCBI36
NG_009061.1:g.25269G>A , LRG_275:g.25269G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1681+152G>A	ENSP00000501161.2:n.1681+152G>A
ENST00000710286.1:c.2038+152G>A	ENSP00000518176.1:n.2038+152G>A
ENST00000673903.1:c.1306+152G>A	ENSP00000501257.1:n.1306+152G>A
ENST00000673913.1:c.421+152G>A	ENSP00000501161.1:n.421+152G>A
ENST00000302118.5:c.1681+152G>A MANE Select	ENSP00000303208.5:n.1681+152G>A
ENST00000490692.1:n.2227+1168G>A
NM_174936.3:c.1681+152G>A , LRG_275t1:c.1681+152G>A	NP_777596.2:n.1681+152G>A
NR_110451.1:n.1288+152G>A
XM_011541193.1:c.802+152G>A	XP_011539495.1:n.802+152G>A
NM_174936.4:c.1681+152G>A MANE Select	NP_777596.2:n.1681+152G>A
NR_110451.2:n.1288+152G>A