Canonical Allele Identifier: CA1565418093
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429282A= , CM000667.2:g.96429282A= GRCh38
NC_000005.9:g.95764986A= , CM000667.1:g.95764986A= GRCh37
NC_000005.8:g.95790742A= NCBI36
NG_021161.1:g.9000T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.216T= MANE Select ENSP00000308024.2:p.His72=
ENST00000311106.7:c.216T= ENSP00000308024.2:p.His72=
ENST00000508626.5:c.75T= ENSP00000421600.1:p.His25=
ENST00000509190.1:c.216T= ENSP00000427294.1:p.His72=
NM_000439.4:c.216T= NP_000430.3:p.His72=
NM_001177875.1:c.75T= NP_001171346.1:p.His25=
NR_130776.1:n.354+49630A=
NM_000439.5:c.216T= MANE Select NP_000430.3:p.His72=
NM_001177875.2:c.75T= NP_001171346.1:p.His25=