Canonical Allele Identifier: CA1565417978
Gene: PCSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429045A= , CM000667.2:g.96429045A= GRCh38
NC_000005.9:g.95764749A= , CM000667.1:g.95764749A= GRCh37
NC_000005.8:g.95790505A= NCBI36
NG_021161.1:g.9237T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.285+168T= MANE Select ENSP00000308024.2:n.285+168T=
ENST00000311106.7:c.285+168T= ENSP00000308024.2:n.285+168T=
ENST00000508626.5:c.144+168T= ENSP00000421600.1:n.144+168T=
ENST00000509190.1:c.285+168T= ENSP00000427294.1:n.285+168T=
NM_000439.4:c.285+168T= NP_000430.3:n.285+168T=
NM_001177875.1:c.144+168T= NP_001171346.1:n.144+168T=
NR_130776.1:n.354+49393A=
NM_000439.5:c.285+168T= MANE Select NP_000430.3:n.285+168T=
NM_001177875.2:c.144+168T= NP_001171346.1:n.144+168T=