Canonical Allele Identifier: CA645586811
Gene: HCN4 HGNC NCBI

Linked Data

COSMIC: COSM368063
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323717_73323718delinsAC , CM000677.2:g.73323717_73323718delinsAC GRCh38
NC_000015.9:g.73616058_73616059delinsAC , CM000677.1:g.73616058_73616059delinsAC GRCh37
NC_000015.8:g.71403111_71403112delinsAC NCBI36
NG_009063.1:g.50547_50548delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2375_2376delinsGT MANE Select ENSP00000261917.3:p.Ala792Gly
ENST00000261917.3:c.2375_2376delinsGT ENSP00000261917.3:p.Ala792Gly
NM_005477.2:c.2375_2376delinsGT NP_005468.1:p.Ala792Gly
XM_011521148.1:c.1157_1158delinsGT XP_011519450.1:p.Ala386Gly
XM_011521148.2:c.1157_1158delinsGT XP_011519450.1:p.Ala386Gly
NM_005477.3:c.2375_2376delinsGT MANE Select NP_005468.1:p.Ala792Gly
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