Canonical Allele Identifier: CA2187185914
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322419_73322420delinsTA , CM000677.2:g.73322419_73322420delinsTA GRCh38
NC_000015.9:g.73614760_73614761delinsTA , CM000677.1:g.73614760_73614761delinsTA GRCh37
NC_000015.8:g.71401813_71401814delinsTA NCBI36
NG_009063.1:g.51845_51846delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*61_*62delinsTA MANE Select ENSP00000261917.3:n.*61_*62delinsTA
ENST00000261917.3:c.*61_*62delinsTA ENSP00000261917.3:n.*61_*62delinsTA
NM_005477.2:c.*61_*62delinsTA NP_005468.1:n.*61_*62delinsTA
XM_011521148.1:c.*61_*62delinsTA XP_011519450.1:n.*61_*62delinsTA
XM_011521148.2:c.*61_*62delinsTA XP_011519450.1:n.*61_*62delinsTA
NM_005477.3:c.*61_*62delinsTA MANE Select NP_005468.1:n.*61_*62delinsTA
Search 100 bp 5'
Search 100 bp 3'