Canonical Allele Identifier: CA2629389836

Gene: HCN4

Linked Data

• gnomAD v4: 15-73367911-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367913del , CM000677.2:g.73367913del	GRCh38
NC_000015.9:g.73660254del , CM000677.1:g.73660254del	GRCh37
NC_000015.8:g.71447307del	NCBI36
NG_009063.1:g.6353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.359del MANE Select	ENSP00000261917.3:p.Gly120AspfsTer?
ENST00000261917.3:c.359del	ENSP00000261917.3:p.Gly120AspfsTer?
NM_005477.2:c.359del	NP_005468.1:p.Gly120AspfsTer?
NM_005477.3:c.359del MANE Select	NP_005468.1:p.Gly120AspfsTer?