Canonical Allele Identifier: CA2629388585
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73329564-TA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329565del , CM000677.2:g.73329565del GRCh38
NC_000015.9:g.73621906del , CM000677.1:g.73621906del GRCh37
NC_000015.8:g.71408959del NCBI36
NG_009063.1:g.44700del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1590+8del MANE Select ENSP00000261917.3:n.1590+8del
ENST00000261917.3:c.1590+8del ENSP00000261917.3:n.1590+8del
NM_005477.2:c.1590+8del NP_005468.1:n.1590+8del
XM_011521148.1:c.372+8del XP_011519450.1:n.372+8del
XM_011521148.2:c.372+8del XP_011519450.1:n.372+8del
NM_005477.3:c.1590+8del MANE Select NP_005468.1:n.1590+8del
Search 100 bp 5'
Search 100 bp 3'