Canonical Allele Identifier: CA619410578
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v2: 15-73615490-ACTCCCCGGGAGGCTGGCCCAGCTGCCCGGGGCTAGATGACGGGGATCTGGATGAGGGTGGGGGTGGCAGGAAGTGCTCCGGGAGTCCCAGGC-A
MyVariant Identifiers: chr15:g.73615491_73615582del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323159_73323250del , CM000677.2:g.73323159_73323250del GRCh38
NC_000015.9:g.73615500_73615591del , CM000677.1:g.73615500_73615591del GRCh37
NC_000015.8:g.71402553_71402644del NCBI36
NG_009063.1:g.51024_51115del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2852_2943del MANE Select ENSP00000261917.3:p.Gly951ValfsTer21
ENST00000261917.3:c.2852_2943del ENSP00000261917.3:p.Gly951ValfsTer21
NM_005477.2:c.2852_2943del NP_005468.1:p.Gly951ValfsTer21
XM_011521148.1:c.1634_1725del XP_011519450.1:p.Gly545ValfsTer21
XM_011521148.2:c.1634_1725del XP_011519450.1:p.Gly545ValfsTer21
NM_005477.3:c.2852_2943del MANE Select NP_005468.1:p.Gly951ValfsTer21
Search 100 bp 5'
Search 100 bp 3'