Canonical Allele Identifier: CA1565401580
Gene: PCSK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96392119T= , CM000667.2:g.96392119T= GRCh38
NC_000005.9:g.95727823T= , CM000667.1:g.95727823T= GRCh37
NC_000005.8:g.95753579T= NCBI36
NG_021161.1:g.46163A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.*882A= MANE Select ENSP00000308024.2:n.*882A=
ENST00000311106.7:c.*882A= ENSP00000308024.2:n.*882A=
NM_000439.4:c.*882A= NP_000430.3:n.*882A=
NM_001177875.1:c.*882A= NP_001171346.1:n.*882A=
NR_130776.1:n.354+12467T=
NM_000439.5:c.*882A= MANE Select NP_000430.3:n.*882A=
NM_001177875.2:c.*882A= NP_001171346.1:n.*882A=
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