Canonical Allele Identifier: CA2629370524
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73322614-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322616del , CM000677.2:g.73322616del GRCh38
NC_000015.9:g.73614957del , CM000677.1:g.73614957del GRCh37
NC_000015.8:g.71402010del NCBI36
NG_009063.1:g.51650del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3478del MANE Select ENSP00000261917.3:p.Ser1160LeufsTer21
ENST00000261917.3:c.3478del ENSP00000261917.3:p.Ser1160LeufsTer21
NM_005477.2:c.3478del NP_005468.1:p.Ser1160LeufsTer21
XM_011521148.1:c.2260del XP_011519450.1:p.Ser754LeufsTer21
XM_011521148.2:c.2260del XP_011519450.1:p.Ser754LeufsTer21
NM_005477.3:c.3478del MANE Select NP_005468.1:p.Ser1160LeufsTer21
Search 100 bp 5'
Search 100 bp 3'