Canonical Allele Identifier: CA2740139585
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059850A>C , CM000663.2:g.55059850A>C GRCh38
NC_000001.10:g.55525523A>C , CM000663.1:g.55525523A>C GRCh37
NC_000001.9:g.55298111A>C NCBI36
NG_009061.1:g.25304A>C , LRG_275:g.25304A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1681+187A>C ENSP00000501161.2:n.1681+187A>C
ENST00000710286.1:c.2038+187A>C ENSP00000518176.1:n.2038+187A>C
ENST00000673903.1:c.1306+187A>C ENSP00000501257.1:n.1306+187A>C
ENST00000673913.1:c.421+187A>C ENSP00000501161.1:n.421+187A>C
ENST00000302118.5:c.1681+187A>C MANE Select ENSP00000303208.5:n.1681+187A>C
ENST00000490692.1:n.2227+1203A>C
NM_174936.3:c.1681+187A>C , LRG_275t1:c.1681+187A>C NP_777596.2:n.1681+187A>C
NR_110451.1:n.1288+187A>C
XM_011541193.1:c.802+187A>C XP_011539495.1:n.802+187A>C
NM_174936.4:c.1681+187A>C MANE Select NP_777596.2:n.1681+187A>C
NR_110451.2:n.1288+187A>C