Canonical Allele Identifier: CA2840286489

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323656del , CM000677.2:g.73323656del	GRCh38
NC_000015.9:g.73615997del , CM000677.1:g.73615997del	GRCh37
NC_000015.8:g.71403050del	NCBI36
NG_009063.1:g.50611del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2439del MANE Select	ENSP00000261917.3:p.Leu814TrpfsTer13
ENST00000261917.3:c.2439del	ENSP00000261917.3:p.Leu814TrpfsTer13
NM_005477.2:c.2439del	NP_005468.1:p.Leu814TrpfsTer13
XM_011521148.1:c.1221del	XP_011519450.1:p.Leu408TrpfsTer13
XM_011521148.2:c.1221del	XP_011519450.1:p.Leu408TrpfsTer13
NM_005477.3:c.2439del MANE Select	NP_005468.1:p.Leu814TrpfsTer13