Canonical Allele Identifier: CA2629389807
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73367634-A-ATTTTTTAAT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367634_73367635insTTTTTTAAT , CM000677.2:g.73367634_73367635insTTTTTTAAT GRCh38
NC_000015.9:g.73659975_73659976insTTTTTTAAT , CM000677.1:g.73659975_73659976insTTTTTTAAT GRCh37
NC_000015.8:g.71447028_71447029insTTTTTTAAT NCBI36
NG_009063.1:g.6630_6631insATTAAAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.636_637insATTAAAAAA MANE Select ENSP00000261917.3:p.Gly212_Phe213insIleLy...
ENST00000261917.3:c.636_637insATTAAAAAA ENSP00000261917.3:p.Gly212_Phe213insIleLy...
NM_005477.2:c.636_637insATTAAAAAA NP_005468.1:p.Gly212_Phe213insIleLysLys
NM_005477.3:c.636_637insATTAAAAAA MANE Select NP_005468.1:p.Gly212_Phe213insIleLysLys
Search 100 bp 5'
Search 100 bp 3'