Canonical Allele Identifier: CA1167981712
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55052754C= , CM000663.2:g.55052754C= GRCh38
NC_000001.10:g.55518427C= , CM000663.1:g.55518427C= GRCh37
NC_000001.9:g.55291015C= NCBI36
NG_009061.1:g.18208C= , LRG_275:g.18208C=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.762C= ENSP00000501161.2:p.Asn254=
ENST00000710286.1:c.1119C= ENSP00000518176.1:p.Asn373=
ENST00000673903.1:c.387C= ENSP00000501257.1:p.Asn129=
ENST00000302118.5:c.762C= MANE Select ENSP00000303208.5:p.Asn254=
ENST00000490692.1:n.1583C=
NM_174936.3:c.762C= , LRG_275t1:c.762C= NP_777596.2:p.Asn254=
NR_110451.1:n.421C=
NM_174936.4:c.762C= MANE Select NP_777596.2:p.Asn254=
NR_110451.2:n.421C=