Canonical Allele Identifier: CA658798404
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 521002
ClinVar RCV Id: RCV000623481
dbSNP Id: rs1555475311
MyVariant Identifiers: chr15:g.73615933_73615934insC (hg19) chr15:g.73323592_73323593insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323592_73323593insC , CM000677.2:g.73323592_73323593insC GRCh38
NC_000015.9:g.73615933_73615934insC , CM000677.1:g.73615933_73615934insC GRCh37
NC_000015.8:g.71402986_71402987insC NCBI36
NG_009063.1:g.50672_50673insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2500_2501insG MANE Select ENSP00000261917.3:p.Pro834ArgfsTer?
ENST00000261917.3:c.2500_2501insG ENSP00000261917.3:p.Pro834ArgfsTer?
NM_005477.2:c.2500_2501insG NP_005468.1:p.Pro834ArgfsTer?
XM_011521148.1:c.1282_1283insG XP_011519450.1:p.Pro428ArgfsTer?
XM_011521148.2:c.1282_1283insG XP_011519450.1:p.Pro428ArgfsTer?
NM_005477.3:c.2500_2501insG MANE Select NP_005468.1:p.Pro834ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'