Canonical Allele Identifier: CA2575783819
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73322893-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322898del , CM000677.2:g.73322898del GRCh38
NC_000015.9:g.73615239del , CM000677.1:g.73615239del GRCh37
NC_000015.8:g.71402292del NCBI36
NG_009063.1:g.51371del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3199del MANE Select ENSP00000261917.3:p.Gln1067SerfsTer?
ENST00000261917.3:c.3199del ENSP00000261917.3:p.Gln1067SerfsTer?
NM_005477.2:c.3199del NP_005468.1:p.Gln1067SerfsTer?
XM_011521148.1:c.1981del XP_011519450.1:p.Gln661SerfsTer?
XM_011521148.2:c.1981del XP_011519450.1:p.Gln661SerfsTer?
NM_005477.3:c.3199del MANE Select NP_005468.1:p.Gln1067SerfsTer?
Search 100 bp 5'
Search 100 bp 3'