Canonical Allele Identifier: CA2629388586
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329567_73329568del , CM000677.2:g.73329567_73329568del GRCh38
NC_000015.9:g.73621908_73621909del , CM000677.1:g.73621908_73621909del GRCh37
NC_000015.8:g.71408961_71408962del NCBI36
NG_009063.1:g.44697_44698del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1590+5_1590+6del MANE Select ENSP00000261917.3:n.1590+5_1590+6del
ENST00000261917.3:c.1590+5_1590+6del ENSP00000261917.3:n.1590+5_1590+6del
NM_005477.2:c.1590+5_1590+6del NP_005468.1:n.1590+5_1590+6del
XM_011521148.1:c.372+5_372+6del XP_011519450.1:n.372+5_372+6del
XM_011521148.2:c.372+5_372+6del XP_011519450.1:n.372+5_372+6del
NM_005477.3:c.1590+5_1590+6del MANE Select NP_005468.1:n.1590+5_1590+6del