Canonical Allele Identifier: CA2804726800
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322389_73322392del , CM000677.2:g.73322389_73322392del GRCh38
NC_000015.9:g.73614730_73614733del , CM000677.1:g.73614730_73614733del GRCh37
NC_000015.8:g.71401783_71401786del NCBI36
NG_009063.1:g.51873_51876del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*89_*92del MANE Select ENSP00000261917.3:n.*89_*92del
ENST00000261917.3:c.*89_*92del ENSP00000261917.3:n.*89_*92del
NM_005477.2:c.*89_*92del NP_005468.1:n.*89_*92del
XM_011521148.1:c.*89_*92del XP_011519450.1:n.*89_*92del
XM_011521148.2:c.*89_*92del XP_011519450.1:n.*89_*92del
NM_005477.3:c.*89_*92del MANE Select NP_005468.1:n.*89_*92del
Search 100 bp 5'
Search 100 bp 3'