Canonical Allele Identifier: CA1565418156
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429414A= , CM000667.2:g.96429414A= GRCh38
NC_000005.9:g.95765118A= , CM000667.1:g.95765118A= GRCh37
NC_000005.8:g.95790874A= NCBI36
NG_021161.1:g.8868T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-97T= MANE Select ENSP00000308024.2:n.181-97T=
ENST00000311106.7:c.181-97T= ENSP00000308024.2:n.181-97T=
ENST00000508626.5:c.40-97T= ENSP00000421600.1:n.40-97T=
ENST00000509190.1:c.181-97T= ENSP00000427294.1:n.181-97T=
NM_000439.4:c.181-97T= NP_000430.3:n.181-97T=
NM_001177875.1:c.40-97T= NP_001171346.1:n.40-97T=
NR_130776.1:n.354+49762A=
NM_000439.5:c.181-97T= MANE Select NP_000430.3:n.181-97T=
NM_001177875.2:c.40-97T= NP_001171346.1:n.40-97T=