Canonical Allele Identifier: CA2804727820

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367817del , CM000677.2:g.73367817del	GRCh38
NC_000015.9:g.73660158del , CM000677.1:g.73660158del	GRCh37
NC_000015.8:g.71447211del	NCBI36
NG_009063.1:g.6450del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.456del MANE Select	ENSP00000261917.3:p.Glu153SerfsTer?
ENST00000261917.3:c.456del	ENSP00000261917.3:p.Glu153SerfsTer?
NM_005477.2:c.456del	NP_005468.1:p.Glu153SerfsTer?
NM_005477.3:c.456del MANE Select	NP_005468.1:p.Glu153SerfsTer?