Canonical Allele Identifier: CA1140125886
Community Standard Title: NM_174936.4(PCSK9):c.523+2637G=
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55049283G= , CM000663.2:g.55049283G= GRCh38
NC_000001.10:g.55514956G= , CM000663.1:g.55514956G= GRCh37
NC_000001.9:g.55287544G= NCBI36
NG_009061.1:g.14737G= , LRG_275:g.14737G=

Transcript Alleles

HGVS Amino-acid Change
NM_174936.4:c.523+2637G= MANE Select NP_777596.2:n.523+2637G=
ENST00000302118.5:c.523+2637G= MANE Select ENSP00000303208.5:n.523+2637G=
NM_174936.3:c.523+2637G= , LRG_275t1:c.523+2637G= NP_777596.2:n.523+2637G=
NR_110451.1:n.183-2995G=
NR_110451.2:n.183-2995G=
ENST00000673726.1:c.524-2060G= ENSP00000501004.1:n.524-2060G=
ENST00000673903.1:c.148+2637G= ENSP00000501257.1:n.148+2637G=
ENST00000673913.2:c.523+2637G= ENSP00000501161.2:n.523+2637G=
ENST00000710286.1:c.880+2637G= ENSP00000518176.1:n.880+2637G=