Canonical Allele Identifier: CA7648935
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 970242
ClinVar RCV Id: RCV001245782 RCV001760282 RCV002484369
dbSNP Id: rs750207209
ExAC: 15:73615544 AGGGTGG / A
gnomAD v2: 15-73615544-AGGGTGG-A
gnomAD v3: 15-73323203-AGGGTGG-A
gnomAD v4: 15-73323203-AGGGTGG-A
MyVariant Identifiers: chr15:g.73615545_73615550del (hg19) chr15:g.73323204_73323209del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323210_73323215del , CM000677.2:g.73323210_73323215del GRCh38
NC_000015.9:g.73615551_73615556del , CM000677.1:g.73615551_73615556del GRCh37
NC_000015.8:g.71402604_71402609del NCBI36
NG_009063.1:g.51056_51061del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2884_2889del MANE Select ENSP00000261917.3:p.Pro962_Pro963del
ENST00000261917.3:c.2884_2889del ENSP00000261917.3:p.Pro962_Pro963del
NM_005477.2:c.2884_2889del NP_005468.1:p.Pro962_Pro963del
XM_011521148.1:c.1666_1671del XP_011519450.1:p.Pro556_Pro557del
XM_011521148.2:c.1666_1671del XP_011519450.1:p.Pro556_Pro557del
NM_005477.3:c.2884_2889del MANE Select NP_005468.1:p.Pro962_Pro963del
Search 100 bp 5'
Search 100 bp 3'