Canonical Allele Identifier: CA2840286490

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323744dup , CM000677.2:g.73323744dup	GRCh38
NC_000015.9:g.73616085dup , CM000677.1:g.73616085dup	GRCh37
NC_000015.8:g.71403138dup	NCBI36
NG_009063.1:g.50522dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2350dup MANE Select	ENSP00000261917.3:p.Ala784GlyfsTer?
ENST00000261917.3:c.2350dup	ENSP00000261917.3:p.Ala784GlyfsTer?
NM_005477.2:c.2350dup	NP_005468.1:p.Ala784GlyfsTer?
XM_011521148.1:c.1132dup	XP_011519450.1:p.Ala378GlyfsTer?
XM_011521148.2:c.1132dup	XP_011519450.1:p.Ala378GlyfsTer?
NM_005477.3:c.2350dup MANE Select	NP_005468.1:p.Ala784GlyfsTer?