Canonical Allele Identifier: CA2629370543

Gene: HCN4

Linked Data

• gnomAD v4: 15-73323028-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323032del , CM000677.2:g.73323032del	GRCh38
NC_000015.9:g.73615373del , CM000677.1:g.73615373del	GRCh37
NC_000015.8:g.71402426del	NCBI36
NG_009063.1:g.51236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3064del MANE Select	ENSP00000261917.3:p.Arg1022GlufsTer?
ENST00000261917.3:c.3064del	ENSP00000261917.3:p.Arg1022GlufsTer?
NM_005477.2:c.3064del	NP_005468.1:p.Arg1022GlufsTer?
XM_011521148.1:c.1846del	XP_011519450.1:p.Arg616GlufsTer?
XM_011521148.2:c.1846del	XP_011519450.1:p.Arg616GlufsTer?
NM_005477.3:c.3064del MANE Select	NP_005468.1:p.Arg1022GlufsTer?