Canonical Allele Identifier: CA715542271
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1245661239
gnomAD v4: 15-73322394-T-TATTG
MyVariant Identifiers: chr15:g.73614735_73614736insATTG (hg19) chr15:g.73322394_73322395insATTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322395_73322398dup , CM000677.2:g.73322395_73322398dup GRCh38
NC_000015.9:g.73614736_73614739dup , CM000677.1:g.73614736_73614739dup GRCh37
NC_000015.8:g.71401789_71401792dup NCBI36
NG_009063.1:g.51867_51870dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*83_*86dup MANE Select ENSP00000261917.3:n.*83_*86dup
ENST00000261917.3:c.*83_*86dup ENSP00000261917.3:n.*83_*86dup
NM_005477.2:c.*83_*86dup NP_005468.1:n.*83_*86dup
XM_011521148.1:c.*83_*86dup XP_011519450.1:n.*83_*86dup
XM_011521148.2:c.*83_*86dup XP_011519450.1:n.*83_*86dup
NM_005477.3:c.*83_*86dup MANE Select NP_005468.1:n.*83_*86dup
Search 100 bp 5'
Search 100 bp 3'