Canonical Allele Identifier: CA2343273730

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154064_55154094delinsTGGGCCCGCAGGTCCAGGGACTCCTTAGCCC , CM000681.2:g.55154064_55154094delinsTGGGCCCGCAGGTCCAGGGACTCCTTAGCCC	GRCh38
NC_000019.9:g.55665432_55665462delinsTGGGCCCGCAGGTCCAGGGACTCCTTAGCCC , CM000681.1:g.55665432_55665462delinsTGGGCCCGCAGGTCCAGGGACTCCTTAGCCC	GRCh37
NC_000019.8:g.60357244_60357274delinsTGGGCCCGCAGGTCCAGGGACTCCTTAGCCC	NCBI36
NG_007866.2:g.8639_8669delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA , LRG_432:g.8639_8669delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA
NG_011829.2:g.145_175delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.485_515delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA MANE Select	ENSP00000341838.5:p.Arg162=
ENST00000665070.1:c.518_548delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA	ENSP00000499482.1:p.Arg173=
ENST00000344887.9:c.485_515delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA	ENSP00000341838.5:p.Arg162=
ENST00000585806.5:n.484_514delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA
ENST00000588882.1:c.410_440delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA	ENSP00000466729.1:p.Arg137=
ENST00000589864.1:n.313_343delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA
NM_000363.4:c.485_515delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA , LRG_432t1:c.485_515delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA	NP_000354.4:p.Arg162=
NM_000363.5:c.485_515delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA MANE Select	NP_000354.4:p.Arg162=