Canonical Allele Identifier: CA619410584
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs749503920
gnomAD v2: 15-73614902-G-GC
gnomAD v4: 15-73322561-G-GC
COSMIC: COSM1285325
MyVariant Identifiers: chr15:g.73614903_73614904insC (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322567dup , CM000677.2:g.73322567dup GRCh38
NC_000015.9:g.73614908dup , CM000677.1:g.73614908dup GRCh37
NC_000015.8:g.71401961dup NCBI36
NG_009063.1:g.51703dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3531dup MANE Select ENSP00000261917.3:p.Pro1178AlafsTer16
ENST00000261917.3:c.3531dup ENSP00000261917.3:p.Pro1178AlafsTer16
NM_005477.2:c.3531dup NP_005468.1:p.Pro1178AlafsTer16
XM_011521148.1:c.2313dup XP_011519450.1:p.Pro772AlafsTer16
XM_011521148.2:c.2313dup XP_011519450.1:p.Pro772AlafsTer16
NM_005477.3:c.3531dup MANE Select NP_005468.1:p.Pro1178AlafsTer16
Search 100 bp 5'
Search 100 bp 3'