Canonical Allele Identifier: CA2187167908

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73330048_73330049delinsTG , CM000677.2:g.73330048_73330049delinsTG	GRCh38
NC_000015.9:g.73622389_73622390delinsTG , CM000677.1:g.73622389_73622390delinsTG	GRCh37
NC_000015.8:g.71409442_71409443delinsTG	NCBI36
NG_009063.1:g.44216_44217delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1372-258_1372-257delinsCA MANE Select	ENSP00000261917.3:n.1372-258_1372-257delinsCA
ENST00000261917.3:c.1372-258_1372-257delinsCA	ENSP00000261917.3:n.1372-258_1372-257delinsCA
NM_005477.2:c.1372-258_1372-257delinsCA	NP_005468.1:n.1372-258_1372-257delinsCA
XM_011521148.1:c.154-258_154-257delinsCA	XP_011519450.1:n.154-258_154-257delinsCA
XM_011521148.2:c.154-258_154-257delinsCA	XP_011519450.1:n.154-258_154-257delinsCA
NM_005477.3:c.1372-258_1372-257delinsCA MANE Select	NP_005468.1:n.1372-258_1372-257delinsCA