Canonical Allele Identifier: CA2575783825
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322971del , CM000677.2:g.73322971del GRCh38
NC_000015.9:g.73615312del , CM000677.1:g.73615312del GRCh37
NC_000015.8:g.71402365del NCBI36
NG_009063.1:g.51297del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3125del MANE Select ENSP00000261917.3:p.Pro1042ArgfsTer?
ENST00000261917.3:c.3125del ENSP00000261917.3:p.Pro1042ArgfsTer?
NM_005477.2:c.3125del NP_005468.1:p.Pro1042ArgfsTer?
XM_011521148.1:c.1907del XP_011519450.1:p.Pro636ArgfsTer?
XM_011521148.2:c.1907del XP_011519450.1:p.Pro636ArgfsTer?
NM_005477.3:c.3125del MANE Select NP_005468.1:p.Pro1042ArgfsTer?