Canonical Allele Identifier: CA1167985818
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061739T= , CM000663.2:g.55061739T= GRCh38
NC_000001.10:g.55527412T= , CM000663.1:g.55527412T= GRCh37
NC_000001.9:g.55300000T= NCBI36
NG_009061.1:g.27193T= , LRG_275:g.27193T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*203+183T= ENSP00000501161.2:n.*203+183T=
ENST00000710286.1:c.2220+183T= ENSP00000518176.1:n.2220+183T=
ENST00000673903.1:c.1488+183T= ENSP00000501257.1:n.1488+183T=
ENST00000673913.1:c.713+183T= ENSP00000501161.1:n.713+183T=
ENST00000302118.5:c.1863+183T= MANE Select ENSP00000303208.5:n.1863+183T=
ENST00000490692.1:n.2409+183T=
NM_174936.3:c.1863+183T= , LRG_275t1:c.1863+183T= NP_777596.2:n.1863+183T=
NR_110451.1:n.1470+183T=
XM_011541193.1:c.984+183T= XP_011539495.1:n.984+183T=
NM_174936.4:c.1863+183T= MANE Select NP_777596.2:n.1863+183T=
NR_110451.2:n.1470+183T=