Canonical Allele Identifier: CA2629389871
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73368094-C-CGAGGGG
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368100_73368105dup , CM000677.2:g.73368100_73368105dup GRCh38
NC_000015.9:g.73660441_73660446dup , CM000677.1:g.73660441_73660446dup GRCh37
NC_000015.8:g.71447494_71447499dup NCBI36
NG_009063.1:g.6165_6170dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.171_176dup MANE Select ENSP00000261917.3:p.Ser59_Ala60insProSer
ENST00000261917.3:c.171_176dup ENSP00000261917.3:p.Ser59_Ala60insProSer
NM_005477.2:c.171_176dup NP_005468.1:p.Ser59_Ala60insProSer
NM_005477.3:c.171_176dup MANE Select NP_005468.1:p.Ser59_Ala60insProSer
Search 100 bp 5'
Search 100 bp 3'