Canonical Allele Identifier: CA2187167890

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73330031_73330036delinsAGGTAC , CM000677.2:g.73330031_73330036delinsAGGTAC	GRCh38
NC_000015.9:g.73622372_73622377delinsAGGTAC , CM000677.1:g.73622372_73622377delinsAGGTAC	GRCh37
NC_000015.8:g.71409425_71409430delinsAGGTAC	NCBI36
NG_009063.1:g.44229_44234delinsGTACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1372-245_1372-240delinsGTACCT MANE Select	ENSP00000261917.3:n.1372-245_1372-240delinsGTACCT
ENST00000261917.3:c.1372-245_1372-240delinsGTACCT	ENSP00000261917.3:n.1372-245_1372-240delinsGTACCT
NM_005477.2:c.1372-245_1372-240delinsGTACCT	NP_005468.1:n.1372-245_1372-240delinsGTACCT
XM_011521148.1:c.154-245_154-240delinsGTACCT	XP_011519450.1:n.154-245_154-240delinsGTACCT
XM_011521148.2:c.154-245_154-240delinsGTACCT	XP_011519450.1:n.154-245_154-240delinsGTACCT
NM_005477.3:c.1372-245_1372-240delinsGTACCT MANE Select	NP_005468.1:n.1372-245_1372-240delinsGTACCT