Canonical Allele Identifier: CA2673782214
Gene: HCN1 HGNC NCBI

Linked Data

gnomAD v4: 5-45645627-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645628del , CM000667.2:g.45645628del GRCh38
NC_000005.9:g.45645730del , CM000667.1:g.45645730del GRCh37
NC_000005.8:g.45681487del NCBI36
NG_042183.1:g.55491del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.426-20del MANE Select ENSP00000307342.4:n.426-20del
ENST00000673735.1:c.426-20del ENSP00000501107.1:n.426-20del
ENST00000303230.5:c.426-20del ENSP00000307342.4:n.426-20del
ENST00000634658.1:c.426-20del ENSP00000489134.1:n.426-20del
NM_021072.3:c.426-20del NP_066550.2:n.426-20del
NM_021072.4:c.426-20del MANE Select NP_066550.2:n.426-20del
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