Canonical Allele Identifier: CA561280130
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs1334074097
gnomAD v2: 5-95727942-A-C
gnomAD v3: 5-96392238-A-C
gnomAD v4: 5-96392238-A-C
MyVariant Identifiers: chr5:g.95727942A>C (hg19) chr5:g.96392238A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96392238A>C , CM000667.2:g.96392238A>C GRCh38
NC_000005.9:g.95727942A>C , CM000667.1:g.95727942A>C GRCh37
NC_000005.8:g.95753698A>C NCBI36
NG_021161.1:g.46044T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.*763T>G MANE Select ENSP00000308024.2:n.*763T>G
ENST00000311106.7:c.*763T>G ENSP00000308024.2:n.*763T>G
NM_000439.4:c.*763T>G NP_000430.3:n.*763T>G
NM_001177875.1:c.*763T>G NP_001171346.1:n.*763T>G
NR_130776.1:n.354+12586A>C
NM_000439.5:c.*763T>G MANE Select NP_000430.3:n.*763T>G
NM_001177875.2:c.*763T>G NP_001171346.1:n.*763T>G
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