Canonical Allele Identifier: CA2673781198
Gene: HCN1 HGNC NCBI

Linked Data

gnomAD v4: 5-45462043-AAT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45462044_45462045del , CM000667.2:g.45462044_45462045del GRCh38
NC_000005.9:g.45462146_45462147del , CM000667.1:g.45462146_45462147del GRCh37
NC_000005.8:g.45497903_45497904del NCBI36
NG_042183.1:g.239074_239075del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.850-38_850-37del MANE Select ENSP00000307342.4:n.850-38_850-37del
ENST00000637305.1:n.13-38_13-37del
ENST00000673735.1:c.850-38_850-37del ENSP00000501107.1:n.850-38_850-37del
ENST00000303230.5:c.850-38_850-37del ENSP00000307342.4:n.850-38_850-37del
NM_021072.3:c.850-38_850-37del NP_066550.2:n.850-38_850-37del
NM_021072.4:c.850-38_850-37del MANE Select NP_066550.2:n.850-38_850-37del
Search 100 bp 5'
Search 100 bp 3'