Canonical Allele Identifier: CA2804726802

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322404del , CM000677.2:g.73322404del	GRCh38
NC_000015.9:g.73614745del , CM000677.1:g.73614745del	GRCh37
NC_000015.8:g.71401798del	NCBI36
NG_009063.1:g.51861del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.*77del MANE Select	ENSP00000261917.3:n.*77del
ENST00000261917.3:c.*77del	ENSP00000261917.3:n.*77del
NM_005477.2:c.*77del	NP_005468.1:n.*77del
XM_011521148.1:c.*77del	XP_011519450.1:n.*77del
XM_011521148.2:c.*77del	XP_011519450.1:n.*77del
NM_005477.3:c.*77del MANE Select	NP_005468.1:n.*77del