Canonical Allele Identifier: CA2343274201

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154945_55154948delinsAAGG , CM000681.2:g.55154945_55154948delinsAAGG	GRCh38
NC_000019.9:g.55666313_55666316delinsAAGG , CM000681.1:g.55666313_55666316delinsAAGG	GRCh37
NC_000019.8:g.60358125_60358128delinsAAGG	NCBI36
NG_007866.2:g.7785_7788delinsCCTT , LRG_432:g.7785_7788delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.283-118_283-115delinsCCTT MANE Select	ENSP00000341838.5:n.283-118_283-115delinsCCTT
ENST00000665070.1:c.283-118_283-115delinsCCTT	ENSP00000499482.1:n.283-118_283-115delinsCCTT
ENST00000344887.9:c.283-118_283-115delinsCCTT	ENSP00000341838.5:n.283-118_283-115delinsCCTT
ENST00000585806.5:n.282-118_282-115delinsCCTT
ENST00000586669.5:n.291-118_291-115delinsCCTT
ENST00000587176.5:n.467-118_467-115delinsCCTT
ENST00000587871.1:c.902-118_902-115delinsCCTT
ENST00000588882.1:c.208-118_208-115delinsCCTT	ENSP00000466729.1:n.208-118_208-115delinsCCTT
ENST00000590463.1:n.455-118_455-115delinsCCTT
NM_000363.4:c.283-118_283-115delinsCCTT , LRG_432t1:c.283-118_283-115delinsCCTT	NP_000354.4:n.283-118_283-115delinsCCTT
NM_000363.5:c.283-118_283-115delinsCCTT MANE Select	NP_000354.4:n.283-118_283-115delinsCCTT