Canonical Allele Identifier: CA2575783957
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332040del , CM000677.2:g.73332040del GRCh38
NC_000015.9:g.73624381del , CM000677.1:g.73624381del GRCh37
NC_000015.8:g.71411434del NCBI36
NG_009063.1:g.42226del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1371+92del MANE Select ENSP00000261917.3:n.1371+92del
ENST00000261917.3:c.1371+92del ENSP00000261917.3:n.1371+92del
NM_005477.2:c.1371+92del NP_005468.1:n.1371+92del
XM_011521148.1:c.153+92del XP_011519450.1:n.153+92del
XM_011521148.2:c.153+92del XP_011519450.1:n.153+92del
NM_005477.3:c.1371+92del MANE Select NP_005468.1:n.1371+92del