Canonical Allele Identifier: CA1565418206
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429521G= , CM000667.2:g.96429521G= GRCh38
NC_000005.9:g.95765225G= , CM000667.1:g.95765225G= GRCh37
NC_000005.8:g.95790981G= NCBI36
NG_021161.1:g.8761C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-204C= MANE Select ENSP00000308024.2:n.181-204C=
ENST00000311106.7:c.181-204C= ENSP00000308024.2:n.181-204C=
ENST00000508626.5:c.40-204C= ENSP00000421600.1:n.40-204C=
ENST00000509190.1:c.181-204C= ENSP00000427294.1:n.181-204C=
NM_000439.4:c.181-204C= NP_000430.3:n.181-204C=
NM_001177875.1:c.40-204C= NP_001171346.1:n.40-204C=
NR_130776.1:n.354+49869G=
NM_000439.5:c.181-204C= MANE Select NP_000430.3:n.181-204C=
NM_001177875.2:c.40-204C= NP_001171346.1:n.40-204C=