Canonical Allele Identifier: CA2841139551

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329660dup , CM000677.2:g.73329660dup	GRCh38
NC_000015.9:g.73622001dup , CM000677.1:g.73622001dup	GRCh37
NC_000015.8:g.71409054dup	NCBI36
NG_009063.1:g.44607dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1505dup MANE Select	ENSP00000261917.3:p.Ala503CysfsTer?
ENST00000261917.3:c.1505dup	ENSP00000261917.3:p.Ala503CysfsTer?
NM_005477.2:c.1505dup	NP_005468.1:p.Ala503CysfsTer?
XM_011521148.1:c.287dup	XP_011519450.1:p.Ala97CysfsTer?
XM_011521148.2:c.287dup	XP_011519450.1:p.Ala97CysfsTer?
NM_005477.3:c.1505dup MANE Select	NP_005468.1:p.Ala503CysfsTer?