Canonical Allele Identifier: CA2629389816
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73367743-G-GGAGGCC
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367745_73367750dup , CM000677.2:g.73367745_73367750dup GRCh38
NC_000015.9:g.73660086_73660091dup , CM000677.1:g.73660086_73660091dup GRCh37
NC_000015.8:g.71447139_71447144dup NCBI36
NG_009063.1:g.6516_6521dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.522_527dup MANE Select ENSP00000261917.3:p.Ser176_Ala177insAlaSer
ENST00000261917.3:c.522_527dup ENSP00000261917.3:p.Ser176_Ala177insAlaSer
NM_005477.2:c.522_527dup NP_005468.1:p.Ser176_Ala177insAlaSer
NM_005477.3:c.522_527dup MANE Select NP_005468.1:p.Ser176_Ala177insAlaSer
Search 100 bp 5'
Search 100 bp 3'