Canonical Allele Identifier: CA2575783818
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322887del , CM000677.2:g.73322887del GRCh38
NC_000015.9:g.73615228del , CM000677.1:g.73615228del GRCh37
NC_000015.8:g.71402281del NCBI36
NG_009063.1:g.51381del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3209del MANE Select ENSP00000261917.3:p.Gly1070AlafsTer?
ENST00000261917.3:c.3209del ENSP00000261917.3:p.Gly1070AlafsTer?
NM_005477.2:c.3209del NP_005468.1:p.Gly1070AlafsTer?
XM_011521148.1:c.1991del XP_011519450.1:p.Gly664AlafsTer?
XM_011521148.2:c.1991del XP_011519450.1:p.Gly664AlafsTer?
NM_005477.3:c.3209del MANE Select NP_005468.1:p.Gly1070AlafsTer?