Canonical Allele Identifier: CA633906489
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs1309845378
gnomAD v2: 19-55665671-TC-T
gnomAD v3: 19-55154303-TC-T
gnomAD v4: 19-55154303-TC-T
MyVariant Identifiers: chr19:g.55665672del (hg19) chr19:g.55154304del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154305del , CM000681.2:g.55154305del GRCh38
NC_000019.9:g.55665673del , CM000681.1:g.55665673del GRCh37
NC_000019.8:g.60357485del NCBI36
NG_007866.2:g.8429del , LRG_432:g.8429del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.373-98del MANE Select ENSP00000341838.5:n.373-98del
ENST00000665070.1:c.406-98del ENSP00000499482.1:n.406-98del
ENST00000344887.9:c.373-98del ENSP00000341838.5:n.373-98del
ENST00000585806.5:n.372-98del
ENST00000586669.5:n.381-98del
ENST00000588882.1:c.298-98del ENSP00000466729.1:n.298-98del
ENST00000589864.1:n.103del
NM_000363.4:c.373-98del , LRG_432t1:c.373-98del NP_000354.4:n.373-98del
NM_000363.5:c.373-98del MANE Select NP_000354.4:n.373-98del
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