Canonical Allele Identifier: CA1167981716
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55052770A= , CM000663.2:g.55052770A= GRCh38
NC_000001.10:g.55518443A= , CM000663.1:g.55518443A= GRCh37
NC_000001.9:g.55291031A= NCBI36
NG_009061.1:g.18224A= , LRG_275:g.18224A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.778A= ENSP00000501161.2:p.Thr260=
ENST00000710286.1:c.1135A= ENSP00000518176.1:p.Thr379=
ENST00000673903.1:c.403A= ENSP00000501257.1:p.Thr135=
ENST00000302118.5:c.778A= MANE Select ENSP00000303208.5:p.Thr260=
ENST00000490692.1:n.1599A=
NM_174936.3:c.778A= , LRG_275t1:c.778A= NP_777596.2:p.Thr260=
NR_110451.1:n.437A=
NM_174936.4:c.778A= MANE Select NP_777596.2:p.Thr260=
NR_110451.2:n.437A=