Canonical Allele Identifier: CA2804727823

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367886del , CM000677.2:g.73367886del	GRCh38
NC_000015.9:g.73660227del , CM000677.1:g.73660227del	GRCh37
NC_000015.8:g.71447280del	NCBI36
NG_009063.1:g.6379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.385del MANE Select	ENSP00000261917.3:p.Arg129GlyfsTer?
ENST00000261917.3:c.385del	ENSP00000261917.3:p.Arg129GlyfsTer?
NM_005477.2:c.385del	NP_005468.1:p.Arg129GlyfsTer?
NM_005477.3:c.385del MANE Select	NP_005468.1:p.Arg129GlyfsTer?