Canonical Allele Identifier: CA2343275058

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156091_55156092delinsAT , CM000681.2:g.55156091_55156092delinsAT	GRCh38
NC_000019.9:g.55667459_55667460delinsAT , CM000681.1:g.55667459_55667460delinsAT	GRCh37
NC_000019.8:g.60359271_60359272delinsAT	NCBI36
NG_007866.2:g.6641_6642delinsAT , LRG_432:g.6641_6642delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.282+109_282+110delinsAT MANE Select	ENSP00000341838.5:n.282+109_282+110delinsAT
ENST00000665070.1:c.282+109_282+110delinsAT	ENSP00000499482.1:n.282+109_282+110delinsAT
ENST00000344887.9:c.282+109_282+110delinsAT	ENSP00000341838.5:n.282+109_282+110delinsAT
ENST00000585806.5:n.281+109_281+110delinsAT
ENST00000586669.5:n.290+109_290+110delinsAT
ENST00000587176.5:n.466+109_466+110delinsAT
ENST00000587871.1:c.901+109_901+110delinsAT
ENST00000588882.1:c.207+109_207+110delinsAT	ENSP00000466729.1:n.207+109_207+110delinsAT
ENST00000590463.1:n.454+109_454+110delinsAT
NM_000363.4:c.282+109_282+110delinsAT , LRG_432t1:c.282+109_282+110delinsAT	NP_000354.4:n.282+109_282+110delinsAT
NM_000363.5:c.282+109_282+110delinsAT MANE Select	NP_000354.4:n.282+109_282+110delinsAT