Canonical Allele Identifier: CA1565401598
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96392139A= , CM000667.2:g.96392139A= GRCh38
NC_000005.9:g.95727843A= , CM000667.1:g.95727843A= GRCh37
NC_000005.8:g.95753599A= NCBI36
NG_021161.1:g.46143T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.*862T= MANE Select ENSP00000308024.2:n.*862T=
ENST00000311106.7:c.*862T= ENSP00000308024.2:n.*862T=
NM_000439.4:c.*862T= NP_000430.3:n.*862T=
NM_001177875.1:c.*862T= NP_001171346.1:n.*862T=
NR_130776.1:n.354+12487A=
NM_000439.5:c.*862T= MANE Select NP_000430.3:n.*862T=
NM_001177875.2:c.*862T= NP_001171346.1:n.*862T=