Canonical Allele Identifier: CA1167984386
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55058469C= , CM000663.2:g.55058469C= GRCh38
NC_000001.10:g.55524142C= , CM000663.1:g.55524142C= GRCh37
NC_000001.9:g.55296730C= NCBI36
NG_009061.1:g.23923C= , LRG_275:g.23923C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1355-30C= ENSP00000501161.2:n.1355-30C=
ENST00000710286.1:c.1712-30C= ENSP00000518176.1:n.1712-30C=
ENST00000673903.1:c.980-30C= ENSP00000501257.1:n.980-30C=
ENST00000673913.1:c.95-30C= ENSP00000501161.1:n.95-30C=
ENST00000302118.5:c.1355-30C= MANE Select ENSP00000303208.5:n.1355-30C=
ENST00000490692.1:n.2079-30C=
NM_174936.3:c.1355-30C= , LRG_275t1:c.1355-30C= NP_777596.2:n.1355-30C=
NR_110451.1:n.962-30C=
XM_011541193.1:c.476-30C= XP_011539495.1:n.476-30C=
NM_174936.4:c.1355-30C= MANE Select NP_777596.2:n.1355-30C=
NR_110451.2:n.962-30C=