Canonical Allele Identifier: CA1167986593
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063644T= , CM000663.2:g.55063644T= GRCh38
NC_000001.10:g.55529317T= , CM000663.1:g.55529317T= GRCh37
NC_000001.9:g.55301905T= NCBI36
NG_009061.1:g.29098T= , LRG_275:g.29098T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*479T= ENSP00000501161.2:n.*479T=
ENST00000710286.1:c.*60T= ENSP00000518176.1:n.*60T=
ENST00000673903.1:c.*60T= ENSP00000501257.1:n.*60T=
ENST00000302118.5:c.*60T= MANE Select ENSP00000303208.5:n.*60T=
ENST00000490692.1:n.2685T=
NM_174936.3:c.*60T= , LRG_275t1:c.*60T= NP_777596.2:n.*60T=
NR_110451.1:n.1746T=
XM_011541193.1:c.*60T= XP_011539495.1:n.*60T=
NM_174936.4:c.*60T= MANE Select NP_777596.2:n.*60T=
NR_110451.2:n.1746T=