Canonical Allele Identifier: CA2629389811

Gene: HCN4

Linked Data

• gnomAD v4: 15-73367669-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367671del , CM000677.2:g.73367671del	GRCh38
NC_000015.9:g.73660012del , CM000677.1:g.73660012del	GRCh37
NC_000015.8:g.71447065del	NCBI36
NG_009063.1:g.6595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.601del MANE Select	ENSP00000261917.3:p.Leu201SerfsTer?
ENST00000261917.3:c.601del	ENSP00000261917.3:p.Leu201SerfsTer?
NM_005477.2:c.601del	NP_005468.1:p.Leu201SerfsTer?
NM_005477.3:c.601del MANE Select	NP_005468.1:p.Leu201SerfsTer?