Canonical Allele Identifier: CA2629370534
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73322900-CCTGGGGTGGTGGGGGG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322905_73322920del , CM000677.2:g.73322905_73322920del GRCh38
NC_000015.9:g.73615246_73615261del , CM000677.1:g.73615246_73615261del GRCh37
NC_000015.8:g.71402299_71402314del NCBI36
NG_009063.1:g.51349_51364del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3177_3192del MANE Select ENSP00000261917.3:p.Ser1059ArgfsTer?
ENST00000261917.3:c.3177_3192del ENSP00000261917.3:p.Ser1059ArgfsTer?
NM_005477.2:c.3177_3192del NP_005468.1:p.Ser1059ArgfsTer?
XM_011521148.1:c.1959_1974del XP_011519450.1:p.Ser653ArgfsTer?
XM_011521148.2:c.1959_1974del XP_011519450.1:p.Ser653ArgfsTer?
NM_005477.3:c.3177_3192del MANE Select NP_005468.1:p.Ser1059ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'