Canonical Allele Identifier: CA971394813
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042876700
gnomAD v3: 15-73323404-C-CTGA
gnomAD v4: 15-73323404-C-CTGA
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323407_73323409dup , CM000677.2:g.73323407_73323409dup GRCh38
NC_000015.9:g.73615748_73615750dup , CM000677.1:g.73615748_73615750dup GRCh37
NC_000015.8:g.71402801_71402803dup NCBI36
NG_009063.1:g.50858_50860dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2686_2688dup MANE Select ENSP00000261917.3:p.Ser896_Ala897insSer
ENST00000261917.3:c.2686_2688dup ENSP00000261917.3:p.Ser896_Ala897insSer
NM_005477.2:c.2686_2688dup NP_005468.1:p.Ser896_Ala897insSer
XM_011521148.1:c.1468_1470dup XP_011519450.1:p.Ser490_Ala491insSer
XM_011521148.2:c.1468_1470dup XP_011519450.1:p.Ser490_Ala491insSer
NM_005477.3:c.2686_2688dup MANE Select NP_005468.1:p.Ser896_Ala897insSer
Search 100 bp 5'
Search 100 bp 3'