Canonical Allele Identifier: CA2629370529

Gene: HCN4

Linked Data

• gnomAD v4: 15-73322788-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322789_73322790dup , CM000677.2:g.73322789_73322790dup	GRCh38
NC_000015.9:g.73615130_73615131dup , CM000677.1:g.73615130_73615131dup	GRCh37
NC_000015.8:g.71402183_71402184dup	NCBI36
NG_009063.1:g.51475_51476dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3303_3304dup MANE Select	ENSP00000261917.3:p.Arg1102ProfsTer?
ENST00000261917.3:c.3303_3304dup	ENSP00000261917.3:p.Arg1102ProfsTer?
NM_005477.2:c.3303_3304dup	NP_005468.1:p.Arg1102ProfsTer?
XM_011521148.1:c.2085_2086dup	XP_011519450.1:p.Arg696ProfsTer?
XM_011521148.2:c.2085_2086dup	XP_011519450.1:p.Arg696ProfsTer?
NM_005477.3:c.3303_3304dup MANE Select	NP_005468.1:p.Arg1102ProfsTer?