Canonical Allele Identifier: CA1565417969
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs1761405373

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429032T>A , CM000667.2:g.96429032T>A GRCh38
NC_000005.9:g.95764736T>A , CM000667.1:g.95764736T>A GRCh37
NC_000005.8:g.95790492T>A NCBI36
NG_021161.1:g.9250A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.285+181A>T MANE Select ENSP00000308024.2:n.285+181A>T
ENST00000311106.7:c.285+181A>T ENSP00000308024.2:n.285+181A>T
ENST00000508626.5:c.144+181A>T ENSP00000421600.1:n.144+181A>T
ENST00000509190.1:c.285+181A>T ENSP00000427294.1:n.285+181A>T
NM_000439.4:c.285+181A>T NP_000430.3:n.285+181A>T
NM_001177875.1:c.144+181A>T NP_001171346.1:n.144+181A>T
NR_130776.1:n.354+49380T>A
NM_000439.5:c.285+181A>T MANE Select NP_000430.3:n.285+181A>T
NM_001177875.2:c.144+181A>T NP_001171346.1:n.144+181A>T