Canonical Allele Identifier: CA1565417013
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96426780A= , CM000667.2:g.96426780A= GRCh38
NC_000005.9:g.95762484A= , CM000667.1:g.95762484A= GRCh37
NC_000005.8:g.95788240A= NCBI36
NG_021161.1:g.11502T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.286-850T= MANE Select ENSP00000308024.2:n.286-850T=
ENST00000311106.7:c.286-850T= ENSP00000308024.2:n.286-850T=
ENST00000508626.5:c.145-850T= ENSP00000421600.1:n.145-850T=
ENST00000509190.1:c.286-850T= ENSP00000427294.1:n.286-850T=
NM_000439.4:c.286-850T= NP_000430.3:n.286-850T=
NM_001177875.1:c.145-850T= NP_001171346.1:n.145-850T=
NR_130776.1:n.354+47128A=
NM_000439.5:c.286-850T= MANE Select NP_000430.3:n.286-850T=
NM_001177875.2:c.145-850T= NP_001171346.1:n.145-850T=