Canonical Allele Identifier: CA2343274104

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154791_55154802delinsCCACCTTGTCCA , CM000681.2:g.55154791_55154802delinsCCACCTTGTCCA	GRCh38
NC_000019.9:g.55666159_55666170delinsCCACCTTGTCCA , CM000681.1:g.55666159_55666170delinsCCACCTTGTCCA	GRCh37
NC_000019.8:g.60357971_60357982delinsCCACCTTGTCCA	NCBI36
NG_007866.2:g.7931_7942delinsTGGACAAGGTGG , LRG_432:g.7931_7942delinsTGGACAAGGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.311_322delinsTGGACAAGGTGG MANE Select	ENSP00000341838.5:p.Val104=
ENST00000665070.1:c.311_322delinsTGGACAAGGTGG	ENSP00000499482.1:p.Val104=
ENST00000344887.9:c.311_322delinsTGGACAAGGTGG	ENSP00000341838.5:p.Val104=
ENST00000585806.5:n.310_321delinsTGGACAAGGTGG
ENST00000586669.5:n.319_330delinsTGGACAAGGTGG
ENST00000587176.5:n.495_506delinsTGGACAAGGTGG
ENST00000587871.1:c.930_941delinsTGGACAAGGTGG
ENST00000588882.1:c.236_247delinsTGGACAAGGTGG	ENSP00000466729.1:p.Val79=
ENST00000590463.1:n.483_494delinsTGGACAAGGTGG
NM_000363.4:c.311_322delinsTGGACAAGGTGG , LRG_432t1:c.311_322delinsTGGACAAGGTGG	NP_000354.4:p.Val104=
NM_000363.5:c.311_322delinsTGGACAAGGTGG MANE Select	NP_000354.4:p.Val104=