Canonical Allele Identifier: CA2343274196

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154940_55154951delinsAGGAGAAGGGGC , CM000681.2:g.55154940_55154951delinsAGGAGAAGGGGC	GRCh38
NC_000019.9:g.55666308_55666319delinsAGGAGAAGGGGC , CM000681.1:g.55666308_55666319delinsAGGAGAAGGGGC	GRCh37
NC_000019.8:g.60358120_60358131delinsAGGAGAAGGGGC	NCBI36
NG_007866.2:g.7782_7793delinsGCCCCTTCTCCT , LRG_432:g.7782_7793delinsGCCCCTTCTCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.283-121_283-110delinsGCCCCTTCTCCT MANE Select	ENSP00000341838.5:n.283-121_283-110delinsGCCCCTTCTCCT
ENST00000665070.1:c.283-121_283-110delinsGCCCCTTCTCCT	ENSP00000499482.1:n.283-121_283-110delinsGCCCCTTCTCCT
ENST00000344887.9:c.283-121_283-110delinsGCCCCTTCTCCT	ENSP00000341838.5:n.283-121_283-110delinsGCCCCTTCTCCT
ENST00000585806.5:n.282-121_282-110delinsGCCCCTTCTCCT
ENST00000586669.5:n.291-121_291-110delinsGCCCCTTCTCCT
ENST00000587176.5:n.467-121_467-110delinsGCCCCTTCTCCT
ENST00000587871.1:c.902-121_902-110delinsGCCCCTTCTCCT
ENST00000588882.1:c.208-121_208-110delinsGCCCCTTCTCCT	ENSP00000466729.1:n.208-121_208-110delinsGCCCCTTCTCCT
ENST00000590463.1:n.455-121_455-110delinsGCCCCTTCTCCT
NM_000363.4:c.283-121_283-110delinsGCCCCTTCTCCT , LRG_432t1:c.283-121_283-110delinsGCCCCTTCTCCT	NP_000354.4:n.283-121_283-110delinsGCCCCTTCTCCT
NM_000363.5:c.283-121_283-110delinsGCCCCTTCTCCT MANE Select	NP_000354.4:n.283-121_283-110delinsGCCCCTTCTCCT