Canonical Allele Identifier: CA2187186699

Gene: HCN4

Linked Data

• dbSNP Id: rs2042869268

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322778_73322779insC , CM000677.2:g.73322778_73322779insC	GRCh38
NC_000015.9:g.73615119_73615120insC , CM000677.1:g.73615119_73615120insC	GRCh37
NC_000015.8:g.71402172_71402173insC	NCBI36
NG_009063.1:g.51486_51487insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.3314_3315insG MANE Select	ENSP00000261917.3:p.His1107AlafsTer?
ENST00000261917.3:c.3314_3315insG	ENSP00000261917.3:p.His1107AlafsTer?
NM_005477.2:c.3314_3315insG	NP_005468.1:p.His1107AlafsTer?
XM_011521148.1:c.2096_2097insG	XP_011519450.1:p.His701AlafsTer?
XM_011521148.2:c.2096_2097insG	XP_011519450.1:p.His701AlafsTer?
NM_005477.3:c.3314_3315insG MANE Select	NP_005468.1:p.His1107AlafsTer?