Canonical Allele Identifier: CA2804714144

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322904_73322906dup , CM000677.2:g.73322904_73322906dup	GRCh38
NC_000015.9:g.73615245_73615247dup , CM000677.1:g.73615245_73615247dup	GRCh37
NC_000015.8:g.71402298_71402300dup	NCBI36
NG_009063.1:g.51360_51362dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3188_3190dup MANE Select	ENSP00000261917.3:p.Pro1063_Gln1064insPro
ENST00000261917.3:c.3188_3190dup	ENSP00000261917.3:p.Pro1063_Gln1064insPro
NM_005477.2:c.3188_3190dup	NP_005468.1:p.Pro1063_Gln1064insPro
XM_011521148.1:c.1970_1972dup	XP_011519450.1:p.Pro657_Gln658insPro
XM_011521148.2:c.1970_1972dup	XP_011519450.1:p.Pro657_Gln658insPro
NM_005477.3:c.3188_3190dup MANE Select	NP_005468.1:p.Pro1063_Gln1064insPro