Canonical Allele Identifier: CA2629389826

Gene: HCN4

Linked Data

• gnomAD v4: 15-73367871-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367873del , CM000677.2:g.73367873del	GRCh38
NC_000015.9:g.73660214del , CM000677.1:g.73660214del	GRCh37
NC_000015.8:g.71447267del	NCBI36
NG_009063.1:g.6393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.399del MANE Select	ENSP00000261917.3:p.Glu134ArgfsTer?
ENST00000261917.3:c.399del	ENSP00000261917.3:p.Glu134ArgfsTer?
NM_005477.2:c.399del	NP_005468.1:p.Glu134ArgfsTer?
NM_005477.3:c.399del MANE Select	NP_005468.1:p.Glu134ArgfsTer?