Canonical Allele Identifier: CA2840701777

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322528dup , CM000677.2:g.73322528dup	GRCh38
NC_000015.9:g.73614869dup , CM000677.1:g.73614869dup	GRCh37
NC_000015.8:g.71401922dup	NCBI36
NG_009063.1:g.51740dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3568dup MANE Select	ENSP00000261917.3:p.Ala1190GlyfsTer4
ENST00000261917.3:c.3568dup	ENSP00000261917.3:p.Ala1190GlyfsTer4
NM_005477.2:c.3568dup	NP_005468.1:p.Ala1190GlyfsTer4
XM_011521148.1:c.2350dup	XP_011519450.1:p.Ala784GlyfsTer4
XM_011521148.2:c.2350dup	XP_011519450.1:p.Ala784GlyfsTer4
NM_005477.3:c.3568dup MANE Select	NP_005468.1:p.Ala1190GlyfsTer4