Canonical Allele Identifier: CA1075717901
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1745525070
gnomAD v3: 5-45645134-TA-T
gnomAD v4: 5-45645134-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645136del , CM000667.2:g.45645136del GRCh38
NC_000005.9:g.45645238del , CM000667.1:g.45645238del GRCh37
NC_000005.8:g.45680995del NCBI36
NG_042183.1:g.55984del

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.849+50del MANE Select ENSP00000307342.4:n.849+50del
ENST00000637256.1:n.77+50del
ENST00000673735.1:c.849+50del ENSP00000501107.1:n.849+50del
ENST00000303230.5:c.849+50del ENSP00000307342.4:n.849+50del
ENST00000634658.1:c.*11del ENSP00000489134.1:n.*11del
NM_021072.3:c.849+50del NP_066550.2:n.849+50del
NM_021072.4:c.849+50del MANE Select NP_066550.2:n.849+50del
Search 100 bp 5'
Search 100 bp 3'