Canonical Allele Identifier: CA2629370539
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73322910-TGGG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322914_73322916del , CM000677.2:g.73322914_73322916del GRCh38
NC_000015.9:g.73615255_73615257del , CM000677.1:g.73615255_73615257del GRCh37
NC_000015.8:g.71402308_71402310del NCBI36
NG_009063.1:g.51352_51354del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3180_3182del MANE Select ENSP00000261917.3:p.Pro1061del
ENST00000261917.3:c.3180_3182del ENSP00000261917.3:p.Pro1061del
NM_005477.2:c.3180_3182del NP_005468.1:p.Pro1061del
XM_011521148.1:c.1962_1964del XP_011519450.1:p.Pro655del
XM_011521148.2:c.1962_1964del XP_011519450.1:p.Pro655del
NM_005477.3:c.3180_3182del MANE Select NP_005468.1:p.Pro1061del
Search 100 bp 5'
Search 100 bp 3'