Canonical Allele Identifier: CA2674667139
Gene: PCSK1 HGNC NCBI

Linked Data

gnomAD v4: 5-96429118-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429118A>C , CM000667.2:g.96429118A>C GRCh38
NC_000005.9:g.95764822A>C , CM000667.1:g.95764822A>C GRCh37
NC_000005.8:g.95790578A>C NCBI36
NG_021161.1:g.9164T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.285+95T>G MANE Select ENSP00000308024.2:n.285+95T>G
ENST00000311106.7:c.285+95T>G ENSP00000308024.2:n.285+95T>G
ENST00000508626.5:c.144+95T>G ENSP00000421600.1:n.144+95T>G
ENST00000509190.1:c.285+95T>G ENSP00000427294.1:n.285+95T>G
NM_000439.4:c.285+95T>G NP_000430.3:n.285+95T>G
NM_001177875.1:c.144+95T>G NP_001171346.1:n.144+95T>G
NR_130776.1:n.354+49466A>C
NM_000439.5:c.285+95T>G MANE Select NP_000430.3:n.285+95T>G
NM_001177875.2:c.144+95T>G NP_001171346.1:n.144+95T>G
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