Canonical Allele Identifier: CA2629370796
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73323792-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323796del , CM000677.2:g.73323796del GRCh38
NC_000015.9:g.73616137del , CM000677.1:g.73616137del GRCh37
NC_000015.8:g.71403190del NCBI36
NG_009063.1:g.50472del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2300del MANE Select ENSP00000261917.3:p.Pro767GlnfsTer11
ENST00000261917.3:c.2300del ENSP00000261917.3:p.Pro767GlnfsTer11
NM_005477.2:c.2300del NP_005468.1:p.Pro767GlnfsTer11
XM_011521148.1:c.1082del XP_011519450.1:p.Pro361GlnfsTer11
XM_011521148.2:c.1082del XP_011519450.1:p.Pro361GlnfsTer11
NM_005477.3:c.2300del MANE Select NP_005468.1:p.Pro767GlnfsTer11
Search 100 bp 5'
Search 100 bp 3'