Canonical Allele Identifier: CA619410588
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1382588344
gnomAD v2: 15-73614970-TTC-T
MyVariant Identifiers: chr15:g.73614971_73614972del (hg19) chr15:g.73322630_73322631del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322630_73322631del , CM000677.2:g.73322630_73322631del GRCh38
NC_000015.9:g.73614971_73614972del , CM000677.1:g.73614971_73614972del GRCh37
NC_000015.8:g.71402024_71402025del NCBI36
NG_009063.1:g.51634_51635del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3462_3463del MANE Select ENSP00000261917.3:p.Lys1155AspfsTer?
ENST00000261917.3:c.3462_3463del ENSP00000261917.3:p.Lys1155AspfsTer?
NM_005477.2:c.3462_3463del NP_005468.1:p.Lys1155AspfsTer?
XM_011521148.1:c.2244_2245del XP_011519450.1:p.Lys749AspfsTer?
XM_011521148.2:c.2244_2245del XP_011519450.1:p.Lys749AspfsTer?
NM_005477.3:c.3462_3463del MANE Select NP_005468.1:p.Lys1155AspfsTer?
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