Canonical Allele Identifier: CA1565402489
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96393208T= , CM000667.2:g.96393208T= GRCh38
NC_000005.9:g.95728912T= , CM000667.1:g.95728912T= GRCh37
NC_000005.8:g.95754668T= NCBI36
NG_021161.1:g.45074A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.2055A= MANE Select ENSP00000308024.2:p.Pro685=
ENST00000311106.7:c.2055A= ENSP00000308024.2:p.Pro685=
ENST00000508626.5:c.1914A= ENSP00000421600.1:p.Pro638=
ENST00000513085.1:n.1198A=
NM_000439.4:c.2055A= NP_000430.3:p.Pro685=
NM_001177875.1:c.1914A= NP_001171346.1:p.Pro638=
NR_130776.1:n.354+13556T=
NM_000439.5:c.2055A= MANE Select NP_000430.3:p.Pro685=
NM_001177875.2:c.1914A= NP_001171346.1:p.Pro638=