Canonical Allele Identifier: CA2629370505
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322467dup , CM000677.2:g.73322467dup GRCh38
NC_000015.9:g.73614808dup , CM000677.1:g.73614808dup GRCh37
NC_000015.8:g.71401861dup NCBI36
NG_009063.1:g.51799dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*15dup MANE Select ENSP00000261917.3:n.*15dup
ENST00000261917.3:c.*15dup ENSP00000261917.3:n.*15dup
NM_005477.2:c.*15dup NP_005468.1:n.*15dup
XM_011521148.1:c.*15dup XP_011519450.1:n.*15dup
XM_011521148.2:c.*15dup XP_011519450.1:n.*15dup
NM_005477.3:c.*15dup MANE Select NP_005468.1:n.*15dup