Canonical Allele Identifier: CA1167984835
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059382G= , CM000663.2:g.55059382G= GRCh38
NC_000001.10:g.55525055G= , CM000663.1:g.55525055G= GRCh37
NC_000001.9:g.55297643G= NCBI36
NG_009061.1:g.24836G= , LRG_275:g.24836G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1504-104G= ENSP00000501161.2:n.1504-104G=
ENST00000710286.1:c.1861-104G= ENSP00000518176.1:n.1861-104G=
ENST00000673903.1:c.1129-104G= ENSP00000501257.1:n.1129-104G=
ENST00000673913.1:c.244-104G= ENSP00000501161.1:n.244-104G=
ENST00000302118.5:c.1504-104G= MANE Select ENSP00000303208.5:n.1504-104G=
ENST00000490692.1:n.2227+735G=
NM_174936.3:c.1504-104G= , LRG_275t1:c.1504-104G= NP_777596.2:n.1504-104G=
NR_110451.1:n.1111-104G=
XM_011541193.1:c.625-104G= XP_011539495.1:n.625-104G=
NM_174936.4:c.1504-104G= MANE Select NP_777596.2:n.1504-104G=
NR_110451.2:n.1111-104G=