Canonical Allele Identifier: CA1565401618
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96392180T= , CM000667.2:g.96392180T= GRCh38
NC_000005.9:g.95727884T= , CM000667.1:g.95727884T= GRCh37
NC_000005.8:g.95753640T= NCBI36
NG_021161.1:g.46102A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.*821A= MANE Select ENSP00000308024.2:n.*821A=
ENST00000311106.7:c.*821A= ENSP00000308024.2:n.*821A=
NM_000439.4:c.*821A= NP_000430.3:n.*821A=
NM_001177875.1:c.*821A= NP_001171346.1:n.*821A=
NR_130776.1:n.354+12528T=
NM_000439.5:c.*821A= MANE Select NP_000430.3:n.*821A=
NM_001177875.2:c.*821A= NP_001171346.1:n.*821A=