Canonical Allele Identifier: CA645586808
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73323052-GC-G
COSMIC: COSM4747471
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323059del , CM000677.2:g.73323059del GRCh38
NC_000015.9:g.73615400del , CM000677.1:g.73615400del GRCh37
NC_000015.8:g.71402453del NCBI36
NG_009063.1:g.51212del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3040del MANE Select ENSP00000261917.3:p.Ala1014LeufsTer4
ENST00000261917.3:c.3040del ENSP00000261917.3:p.Ala1014LeufsTer4
NM_005477.2:c.3040del NP_005468.1:p.Ala1014LeufsTer4
XM_011521148.1:c.1822del XP_011519450.1:p.Ala608LeufsTer4
XM_011521148.2:c.1822del XP_011519450.1:p.Ala608LeufsTer4
NM_005477.3:c.3040del MANE Select NP_005468.1:p.Ala1014LeufsTer4
Search 100 bp 5'
Search 100 bp 3'