Canonical Allele Identifier: CA2841828647
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059446dup , CM000663.2:g.55059446dup GRCh38
NC_000001.10:g.55525119dup , CM000663.1:g.55525119dup GRCh37
NC_000001.9:g.55297707dup NCBI36
NG_009061.1:g.24900dup , LRG_275:g.24900dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1504-40dup ENSP00000501161.2:n.1504-40dup
ENST00000710286.1:c.1861-40dup ENSP00000518176.1:n.1861-40dup
ENST00000673903.1:c.1129-40dup ENSP00000501257.1:n.1129-40dup
ENST00000673913.1:c.244-40dup ENSP00000501161.1:n.244-40dup
ENST00000302118.5:c.1504-40dup MANE Select ENSP00000303208.5:n.1504-40dup
ENST00000490692.1:n.2227+799dup
NM_174936.3:c.1504-40dup , LRG_275t1:c.1504-40dup NP_777596.2:n.1504-40dup
NR_110451.1:n.1111-40dup
XM_011541193.1:c.625-40dup XP_011539495.1:n.625-40dup
NM_174936.4:c.1504-40dup MANE Select NP_777596.2:n.1504-40dup
NR_110451.2:n.1111-40dup