Canonical Allele Identifier: CA1565411976
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96416032C= , CM000667.2:g.96416032C= GRCh38
NC_000005.9:g.95751736C= , CM000667.1:g.95751736C= GRCh37
NC_000005.8:g.95777492C= NCBI36
NG_021161.1:g.22250G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.709+1G= MANE Select ENSP00000308024.2:n.709+1G=
ENST00000311106.7:c.709+1G= ENSP00000308024.2:n.709+1G=
ENST00000508626.5:c.568+1G= ENSP00000421600.1:n.568+1G=
NM_000439.4:c.709+1G= NP_000430.3:n.709+1G=
NM_001177875.1:c.568+1G= NP_001171346.1:n.568+1G=
NR_130776.1:n.354+36380C=
NM_000439.5:c.709+1G= MANE Select NP_000430.3:n.709+1G=
NM_001177875.2:c.568+1G= NP_001171346.1:n.568+1G=