Canonical Allele Identifier: CA1565418083
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429254T= , CM000667.2:g.96429254T= GRCh38
NC_000005.9:g.95764958T= , CM000667.1:g.95764958T= GRCh37
NC_000005.8:g.95790714T= NCBI36
NG_021161.1:g.9028A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.244A= MANE Select ENSP00000308024.2:p.Ser82=
ENST00000311106.7:c.244A= ENSP00000308024.2:p.Ser82=
ENST00000508626.5:c.103A= ENSP00000421600.1:p.Ser35=
ENST00000509190.1:c.244A= ENSP00000427294.1:p.Ser82=
NM_000439.4:c.244A= NP_000430.3:p.Ser82=
NM_001177875.1:c.103A= NP_001171346.1:p.Ser35=
NR_130776.1:n.354+49602T=
NM_000439.5:c.244A= MANE Select NP_000430.3:p.Ser82=
NM_001177875.2:c.103A= NP_001171346.1:p.Ser35=