Canonical Allele Identifier: CA2187186569

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322721_73322722delinsAC , CM000677.2:g.73322721_73322722delinsAC	GRCh38
NC_000015.9:g.73615062_73615063delinsAC , CM000677.1:g.73615062_73615063delinsAC	GRCh37
NC_000015.8:g.71402115_71402116delinsAC	NCBI36
NG_009063.1:g.51543_51544delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3371_3372delinsGT MANE Select	ENSP00000261917.3:p.Gly1124=
ENST00000261917.3:c.3371_3372delinsGT	ENSP00000261917.3:p.Gly1124=
NM_005477.2:c.3371_3372delinsGT	NP_005468.1:p.Gly1124=
XM_011521148.1:c.2153_2154delinsGT	XP_011519450.1:p.Gly718=
XM_011521148.2:c.2153_2154delinsGT	XP_011519450.1:p.Gly718=
NM_005477.3:c.3371_3372delinsGT MANE Select	NP_005468.1:p.Gly1124=