Canonical Allele Identifier: CA2838397514

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73368076dup , CM000677.2:g.73368076dup	GRCh38
NC_000015.9:g.73660417dup , CM000677.1:g.73660417dup	GRCh37
NC_000015.8:g.71447470dup	NCBI36
NG_009063.1:g.6190dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.196dup MANE Select	ENSP00000261917.3:p.Glu66GlyfsTer?
ENST00000261917.3:c.196dup	ENSP00000261917.3:p.Glu66GlyfsTer?
NM_005477.2:c.196dup	NP_005468.1:p.Glu66GlyfsTer?
NM_005477.3:c.196dup MANE Select	NP_005468.1:p.Glu66GlyfsTer?