Canonical Allele Identifier: CA1565418078
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429231T= , CM000667.2:g.96429231T= GRCh38
NC_000005.9:g.95764935T= , CM000667.1:g.95764935T= GRCh37
NC_000005.8:g.95790691T= NCBI36
NG_021161.1:g.9051A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.267A= MANE Select ENSP00000308024.2:p.Arg89=
ENST00000311106.7:c.267A= ENSP00000308024.2:p.Arg89=
ENST00000508626.5:c.126A= ENSP00000421600.1:p.Arg42=
ENST00000509190.1:c.267A= ENSP00000427294.1:p.Arg89=
NM_000439.4:c.267A= NP_000430.3:p.Arg89=
NM_001177875.1:c.126A= NP_001171346.1:p.Arg42=
NR_130776.1:n.354+49579T=
NM_000439.5:c.267A= MANE Select NP_000430.3:p.Arg89=
NM_001177875.2:c.126A= NP_001171346.1:p.Arg42=