Canonical Allele Identifier: CA3350217
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs770227055
gnomAD v2: 5-95734782-A-G
gnomAD v4: 5-96399078-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96399078A>G , CM000667.2:g.96399078A>G GRCh38
NC_000005.9:g.95734782A>G , CM000667.1:g.95734782A>G GRCh37
NC_000005.8:g.95760538A>G NCBI36
NG_021161.1:g.39204T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.1431-42T>C MANE Select ENSP00000308024.2:n.1431-42T>C
ENST00000311106.7:c.1431-42T>C ENSP00000308024.2:n.1431-42T>C
ENST00000508626.5:c.1290-42T>C ENSP00000421600.1:n.1290-42T>C
ENST00000513085.1:n.574-42T>C
NM_000439.4:c.1431-42T>C NP_000430.3:n.1431-42T>C
NM_001177875.1:c.1290-42T>C NP_001171346.1:n.1290-42T>C
NR_130776.1:n.354+19426A>G
NM_000439.5:c.1431-42T>C MANE Select NP_000430.3:n.1431-42T>C
NM_001177875.2:c.1290-42T>C NP_001171346.1:n.1290-42T>C