Canonical Allele Identifier: CA2578305113
Gene: HCN1 HGNC NCBI

Linked Data

gnomAD v4: 5-45645123-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645127del , CM000667.2:g.45645127del GRCh38
NC_000005.9:g.45645229del , CM000667.1:g.45645229del GRCh37
NC_000005.8:g.45680986del NCBI36
NG_042183.1:g.55995del

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.849+61del MANE Select ENSP00000307342.4:n.849+61del
ENST00000637256.1:n.77+61del
ENST00000673735.1:c.849+61del ENSP00000501107.1:n.849+61del
ENST00000303230.5:c.849+61del ENSP00000307342.4:n.849+61del
ENST00000634658.1:c.*22del ENSP00000489134.1:n.*22del
NM_021072.3:c.849+61del NP_066550.2:n.849+61del
NM_021072.4:c.849+61del MANE Select NP_066550.2:n.849+61del
Search 100 bp 5'
Search 100 bp 3'