Canonical Allele Identifier: CA2841139547

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329552dup , CM000677.2:g.73329552dup	GRCh38
NC_000015.9:g.73621893dup , CM000677.1:g.73621893dup	GRCh37
NC_000015.8:g.71408946dup	NCBI36
NG_009063.1:g.44715dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1590+23dup MANE Select	ENSP00000261917.3:n.1590+23dup
ENST00000261917.3:c.1590+23dup	ENSP00000261917.3:n.1590+23dup
NM_005477.2:c.1590+23dup	NP_005468.1:n.1590+23dup
XM_011521148.1:c.372+23dup	XP_011519450.1:n.372+23dup
XM_011521148.2:c.372+23dup	XP_011519450.1:n.372+23dup
NM_005477.3:c.1590+23dup MANE Select	NP_005468.1:n.1590+23dup