Canonical Allele Identifier: CA2575783829
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323049del , CM000677.2:g.73323049del GRCh38
NC_000015.9:g.73615390del , CM000677.1:g.73615390del GRCh37
NC_000015.8:g.71402443del NCBI36
NG_009063.1:g.51219del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3047del MANE Select ENSP00000261917.3:p.Pro1016LeufsTer2
ENST00000261917.3:c.3047del ENSP00000261917.3:p.Pro1016LeufsTer2
NM_005477.2:c.3047del NP_005468.1:p.Pro1016LeufsTer2
XM_011521148.1:c.1829del XP_011519450.1:p.Pro610LeufsTer2
XM_011521148.2:c.1829del XP_011519450.1:p.Pro610LeufsTer2
NM_005477.3:c.3047del MANE Select NP_005468.1:p.Pro1016LeufsTer2