Canonical Allele Identifier: CA122898597
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs77150784

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96392175T>G , CM000667.2:g.96392175T>G GRCh38
NC_000005.9:g.95727879T>G , CM000667.1:g.95727879T>G GRCh37
NC_000005.8:g.95753635T>G NCBI36
NG_021161.1:g.46107A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.*826A>C MANE Select ENSP00000308024.2:n.*826A>C
ENST00000311106.7:c.*826A>C ENSP00000308024.2:n.*826A>C
NM_000439.4:c.*826A>C NP_000430.3:n.*826A>C
NM_001177875.1:c.*826A>C NP_001171346.1:n.*826A>C
NR_130776.1:n.354+12523T>G
NM_000439.5:c.*826A>C MANE Select NP_000430.3:n.*826A>C
NM_001177875.2:c.*826A>C NP_001171346.1:n.*826A>C