Canonical Allele Identifier: CA2629389835
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73367894-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367895del , CM000677.2:g.73367895del GRCh38
NC_000015.9:g.73660236del , CM000677.1:g.73660236del GRCh37
NC_000015.8:g.71447289del NCBI36
NG_009063.1:g.6370del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.376del MANE Select ENSP00000261917.3:p.Ala126ArgfsTer?
ENST00000261917.3:c.376del ENSP00000261917.3:p.Ala126ArgfsTer?
NM_005477.2:c.376del NP_005468.1:p.Ala126ArgfsTer?
NM_005477.3:c.376del MANE Select NP_005468.1:p.Ala126ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'