Canonical Allele Identifier: CA1565417966
Gene: PCSK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429027C= , CM000667.2:g.96429027C= GRCh38
NC_000005.9:g.95764731C= , CM000667.1:g.95764731C= GRCh37
NC_000005.8:g.95790487C= NCBI36
NG_021161.1:g.9255G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.285+186G= MANE Select ENSP00000308024.2:n.285+186G=
ENST00000311106.7:c.285+186G= ENSP00000308024.2:n.285+186G=
ENST00000508626.5:c.144+186G= ENSP00000421600.1:n.144+186G=
ENST00000509190.1:c.285+186G= ENSP00000427294.1:n.285+186G=
NM_000439.4:c.285+186G= NP_000430.3:n.285+186G=
NM_001177875.1:c.144+186G= NP_001171346.1:n.144+186G=
NR_130776.1:n.354+49375C=
NM_000439.5:c.285+186G= MANE Select NP_000430.3:n.285+186G=
NM_001177875.2:c.144+186G= NP_001171346.1:n.144+186G=
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