Canonical Allele Identifier: CA1565401632
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96392205C= , CM000667.2:g.96392205C= GRCh38
NC_000005.9:g.95727909C= , CM000667.1:g.95727909C= GRCh37
NC_000005.8:g.95753665C= NCBI36
NG_021161.1:g.46077G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.*796G= MANE Select ENSP00000308024.2:n.*796G=
ENST00000311106.7:c.*796G= ENSP00000308024.2:n.*796G=
NM_000439.4:c.*796G= NP_000430.3:n.*796G=
NM_001177875.1:c.*796G= NP_001171346.1:n.*796G=
NR_130776.1:n.354+12553C=
NM_000439.5:c.*796G= MANE Select NP_000430.3:n.*796G=
NM_001177875.2:c.*796G= NP_001171346.1:n.*796G=