Canonical Allele Identifier: CA2629389823
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367854_73367855insA , CM000677.2:g.73367854_73367855insA GRCh38
NC_000015.9:g.73660195_73660196insA , CM000677.1:g.73660195_73660196insA GRCh37
NC_000015.8:g.71447248_71447249insA NCBI36
NG_009063.1:g.6410_6411insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.416_417insT MANE Select ENSP00000261917.3:p.Gly140ArgfsTer?
ENST00000261917.3:c.416_417insT ENSP00000261917.3:p.Gly140ArgfsTer?
NM_005477.2:c.416_417insT NP_005468.1:p.Gly140ArgfsTer?
NM_005477.3:c.416_417insT MANE Select NP_005468.1:p.Gly140ArgfsTer?