Canonical Allele Identifier: CA2575783828
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73323009-A-AG
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323015dup , CM000677.2:g.73323015dup GRCh38
NC_000015.9:g.73615356dup , CM000677.1:g.73615356dup GRCh37
NC_000015.8:g.71402409dup NCBI36
NG_009063.1:g.51255dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3083dup MANE Select ENSP00000261917.3:p.Gly1029TrpfsTer?
ENST00000261917.3:c.3083dup ENSP00000261917.3:p.Gly1029TrpfsTer?
NM_005477.2:c.3083dup NP_005468.1:p.Gly1029TrpfsTer?
XM_011521148.1:c.1865dup XP_011519450.1:p.Gly623TrpfsTer?
XM_011521148.2:c.1865dup XP_011519450.1:p.Gly623TrpfsTer?
NM_005477.3:c.3083dup MANE Select NP_005468.1:p.Gly1029TrpfsTer?
Search 100 bp 5'
Search 100 bp 3'