Canonical Allele Identifier: CA1167984822
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059347C= , CM000663.2:g.55059347C= GRCh38
NC_000001.10:g.55525020C= , CM000663.1:g.55525020C= GRCh37
NC_000001.9:g.55297608C= NCBI36
NG_009061.1:g.24801C= , LRG_275:g.24801C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1504-139C= ENSP00000501161.2:n.1504-139C=
ENST00000710286.1:c.1861-139C= ENSP00000518176.1:n.1861-139C=
ENST00000673903.1:c.1129-139C= ENSP00000501257.1:n.1129-139C=
ENST00000673913.1:c.244-139C= ENSP00000501161.1:n.244-139C=
ENST00000302118.5:c.1504-139C= MANE Select ENSP00000303208.5:n.1504-139C=
ENST00000490692.1:n.2227+700C=
NM_174936.3:c.1504-139C= , LRG_275t1:c.1504-139C= NP_777596.2:n.1504-139C=
NR_110451.1:n.1111-139C=
XM_011541193.1:c.625-139C= XP_011539495.1:n.625-139C=
NM_174936.4:c.1504-139C= MANE Select NP_777596.2:n.1504-139C=
NR_110451.2:n.1111-139C=