Canonical Allele Identifier: CA2187167727

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329803_73329804delinsCG , CM000677.2:g.73329803_73329804delinsCG	GRCh38
NC_000015.9:g.73622144_73622145delinsCG , CM000677.1:g.73622144_73622145delinsCG	GRCh37
NC_000015.8:g.71409197_71409198delinsCG	NCBI36
NG_009063.1:g.44461_44462delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1372-13_1372-12delinsCG MANE Select	ENSP00000261917.3:n.1372-13_1372-12delinsCG
ENST00000261917.3:c.1372-13_1372-12delinsCG	ENSP00000261917.3:n.1372-13_1372-12delinsCG
NM_005477.2:c.1372-13_1372-12delinsCG	NP_005468.1:n.1372-13_1372-12delinsCG
XM_011521148.1:c.154-13_154-12delinsCG	XP_011519450.1:n.154-13_154-12delinsCG
XM_011521148.2:c.154-13_154-12delinsCG	XP_011519450.1:n.154-13_154-12delinsCG
NM_005477.3:c.1372-13_1372-12delinsCG MANE Select	NP_005468.1:n.1372-13_1372-12delinsCG