Canonical Allele Identifier: CA2187167804

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329897_73329898delinsGC , CM000677.2:g.73329897_73329898delinsGC	GRCh38
NC_000015.9:g.73622238_73622239delinsGC , CM000677.1:g.73622238_73622239delinsGC	GRCh37
NC_000015.8:g.71409291_71409292delinsGC	NCBI36
NG_009063.1:g.44367_44368delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1372-107_1372-106delinsGC MANE Select	ENSP00000261917.3:n.1372-107_1372-106delinsGC
ENST00000261917.3:c.1372-107_1372-106delinsGC	ENSP00000261917.3:n.1372-107_1372-106delinsGC
NM_005477.2:c.1372-107_1372-106delinsGC	NP_005468.1:n.1372-107_1372-106delinsGC
XM_011521148.1:c.154-107_154-106delinsGC	XP_011519450.1:n.154-107_154-106delinsGC
XM_011521148.2:c.154-107_154-106delinsGC	XP_011519450.1:n.154-107_154-106delinsGC
NM_005477.3:c.1372-107_1372-106delinsGC MANE Select	NP_005468.1:n.1372-107_1372-106delinsGC