Canonical Allele Identifier: CA1565417031
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96426806C= , CM000667.2:g.96426806C= GRCh38
NC_000005.9:g.95762510C= , CM000667.1:g.95762510C= GRCh37
NC_000005.8:g.95788266C= NCBI36
NG_021161.1:g.11476G=

Transcript Alleles

HGVS Amino-acid change
ENST00000311106.8:c.286-876G= MANE Select ENSP00000308024.2:n.286-876G=
ENST00000311106.7:c.286-876G= ENSP00000308024.2:n.286-876G=
ENST00000508626.5:c.145-876G= ENSP00000421600.1:n.145-876G=
ENST00000509190.1:c.286-876G= ENSP00000427294.1:n.286-876G=
NM_000439.4:c.286-876G= NP_000430.3:n.286-876G=
NM_001177875.1:c.145-876G= NP_001171346.1:n.145-876G=
NR_130776.1:n.354+47154C=
NM_000439.5:c.286-876G= MANE Select NP_000430.3:n.286-876G=
NM_001177875.2:c.145-876G= NP_001171346.1:n.145-876G=