Canonical Allele Identifier: CA1565418239
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429563C= , CM000667.2:g.96429563C= GRCh38
NC_000005.9:g.95765267C= , CM000667.1:g.95765267C= GRCh37
NC_000005.8:g.95791023C= NCBI36
NG_021161.1:g.8719G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-246G= MANE Select ENSP00000308024.2:n.181-246G=
ENST00000311106.7:c.181-246G= ENSP00000308024.2:n.181-246G=
ENST00000508626.5:c.40-246G= ENSP00000421600.1:n.40-246G=
ENST00000509190.1:c.181-246G= ENSP00000427294.1:n.181-246G=
NM_000439.4:c.181-246G= NP_000430.3:n.181-246G=
NM_001177875.1:c.40-246G= NP_001171346.1:n.40-246G=
NR_130776.1:n.354+49911C=
NM_000439.5:c.181-246G= MANE Select NP_000430.3:n.181-246G=
NM_001177875.2:c.40-246G= NP_001171346.1:n.40-246G=