Canonical Allele Identifier: CA272664570

Gene: HCN4

Linked Data

• dbSNP Id: rs71442382

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323501_73323502delinsAA , CM000677.2:g.73323501_73323502delinsAA	GRCh38
NC_000015.9:g.73615842_73615843delinsAA , CM000677.1:g.73615842_73615843delinsAA	GRCh37
NC_000015.8:g.71402895_71402896delinsAA	NCBI36
NG_009063.1:g.50763_50764delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2591_2592delinsTT MANE Select	ENSP00000261917.3:p.Gly864Val
ENST00000261917.3:c.2591_2592delinsTT	ENSP00000261917.3:p.Gly864Val
NM_005477.2:c.2591_2592delinsTT	NP_005468.1:p.Gly864Val
XM_011521148.1:c.1373_1374delinsTT	XP_011519450.1:p.Gly458Val
XM_011521148.2:c.1373_1374delinsTT	XP_011519450.1:p.Gly458Val
NM_005477.3:c.2591_2592delinsTT MANE Select	NP_005468.1:p.Gly864Val