Canonical Allele Identifier: CA1167985759
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061591C= , CM000663.2:g.55061591C= GRCh38
NC_000001.10:g.55527264C= , CM000663.1:g.55527264C= GRCh37
NC_000001.9:g.55299852C= NCBI36
NG_009061.1:g.27045C= , LRG_275:g.27045C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*203+35C= ENSP00000501161.2:n.*203+35C=
ENST00000710286.1:c.2220+35C= ENSP00000518176.1:n.2220+35C=
ENST00000673903.1:c.1488+35C= ENSP00000501257.1:n.1488+35C=
ENST00000673913.1:c.713+35C= ENSP00000501161.1:n.713+35C=
ENST00000302118.5:c.1863+35C= MANE Select ENSP00000303208.5:n.1863+35C=
ENST00000490692.1:n.2409+35C=
NM_174936.3:c.1863+35C= , LRG_275t1:c.1863+35C= NP_777596.2:n.1863+35C=
NR_110451.1:n.1470+35C=
XM_011541193.1:c.984+35C= XP_011539495.1:n.984+35C=
NM_174936.4:c.1863+35C= MANE Select NP_777596.2:n.1863+35C=
NR_110451.2:n.1470+35C=