Canonical Allele Identifier: CA2804726812

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322734_73322767del , CM000677.2:g.73322734_73322767del	GRCh38
NC_000015.9:g.73615075_73615108del , CM000677.1:g.73615075_73615108del	GRCh37
NC_000015.8:g.71402128_71402161del	NCBI36
NG_009063.1:g.51503_51536del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3331_3364del MANE Select	ENSP00000261917.3:p.Glu1111LeufsTer?
ENST00000261917.3:c.3331_3364del	ENSP00000261917.3:p.Glu1111LeufsTer?
NM_005477.2:c.3331_3364del	NP_005468.1:p.Glu1111LeufsTer?
XM_011521148.1:c.2113_2146del	XP_011519450.1:p.Glu705LeufsTer?
XM_011521148.2:c.2113_2146del	XP_011519450.1:p.Glu705LeufsTer?
NM_005477.3:c.3331_3364del MANE Select	NP_005468.1:p.Glu1111LeufsTer?