Canonical Allele Identifier: CA2629370530
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73322800-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322804del , CM000677.2:g.73322804del GRCh38
NC_000015.9:g.73615145del , CM000677.1:g.73615145del GRCh37
NC_000015.8:g.71402198del NCBI36
NG_009063.1:g.51464del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3292del MANE Select ENSP00000261917.3:p.Ala1098ArgfsTer?
ENST00000261917.3:c.3292del ENSP00000261917.3:p.Ala1098ArgfsTer?
NM_005477.2:c.3292del NP_005468.1:p.Ala1098ArgfsTer?
XM_011521148.1:c.2074del XP_011519450.1:p.Ala692ArgfsTer?
XM_011521148.2:c.2074del XP_011519450.1:p.Ala692ArgfsTer?
NM_005477.3:c.3292del MANE Select NP_005468.1:p.Ala1098ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'