Canonical Allele Identifier: CA2674667237
Gene: PCSK1 HGNC NCBI

Linked Data

gnomAD v4: 5-96429394-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429396del , CM000667.2:g.96429396del GRCh38
NC_000005.9:g.95765100del , CM000667.1:g.95765100del GRCh37
NC_000005.8:g.95790856del NCBI36
NG_021161.1:g.8887del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-78del MANE Select ENSP00000308024.2:n.181-78del
ENST00000311106.7:c.181-78del ENSP00000308024.2:n.181-78del
ENST00000508626.5:c.40-78del ENSP00000421600.1:n.40-78del
ENST00000509190.1:c.181-78del ENSP00000427294.1:n.181-78del
NM_000439.4:c.181-78del NP_000430.3:n.181-78del
NM_001177875.1:c.40-78del NP_001171346.1:n.40-78del
NR_130776.1:n.354+49744del
NM_000439.5:c.181-78del MANE Select NP_000430.3:n.181-78del
NM_001177875.2:c.40-78del NP_001171346.1:n.40-78del
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