Canonical Allele Identifier: CA1565411980
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96416041T= , CM000667.2:g.96416041T= GRCh38
NC_000005.9:g.95751745T= , CM000667.1:g.95751745T= GRCh37
NC_000005.8:g.95777501T= NCBI36
NG_021161.1:g.22241A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.701A= MANE Select ENSP00000308024.2:p.Lys234=
ENST00000311106.7:c.701A= ENSP00000308024.2:p.Lys234=
ENST00000508626.5:c.560A= ENSP00000421600.1:p.Lys187=
NM_000439.4:c.701A= NP_000430.3:p.Lys234=
NM_001177875.1:c.560A= NP_001171346.1:p.Lys187=
NR_130776.1:n.354+36389T=
NM_000439.5:c.701A= MANE Select NP_000430.3:p.Lys234=
NM_001177875.2:c.560A= NP_001171346.1:p.Lys187=