Canonical Allele Identifier: CA2546555172

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55153730_55153731insAAAAAAAAAAAAAAAAAGGAAATAAAAAAAAAATTTTTTTTAAACCT , CM000681.2:g.55153730_55153731insAAAAAAAAAAAAAAAAAGGAAATAAAAAAAAAATTTTTTTTAAACCT	GRCh38
NC_000019.9:g.55665098_55665099insAAAAAAAAAAAAAAAAAGGAAATAAAAAAAAAATTTTTTTTAAACCT , CM000681.1:g.55665098_55665099insAAAAAAAAAAAAAAAAAGGAAATAAAAAAAAAATTTTTTTTAAACCT	GRCh37
NC_000019.8:g.60356910_60356911insAAAAAAAAAAAAAAAAAGGAAATAAAAAAAAAATTTTTTTTAAACCT	NCBI36
NG_007866.2:g.9002_9003insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT , LRG_432:g.9002_9003insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT
NG_011829.2:g.508_509insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.549+299_549+300insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT MANE Select	ENSP00000341838.5:n.549+299_549+300insAGGTTTAAAAAAAATTTTTTTTT...
ENST00000665070.1:c.582+299_582+300insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT	ENSP00000499482.1:n.582+299_582+300insAGGTTTAAAAAAAATTTTTTTTT...
ENST00000344887.9:c.549+299_549+300insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT	ENSP00000341838.5:n.549+299_549+300insAGGTTTAAAAAAAATTTTTTTTT...
ENST00000585806.5:n.548+299_548+300insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT
ENST00000588882.1:c.474+299_474+300insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT	ENSP00000466729.1:n.474+299_474+300insAGGTTTAAAAAAAATTTTTTTTT...
ENST00000589864.1:n.377+299_377+300insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT
NM_000363.4:c.549+299_549+300insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT , LRG_432t1:c.549+299_549+300insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT	NP_000354.4:n.549+299_549+300insAGGTTTAAAAAAAATTTTTTTTTTATTTC...
NM_000363.5:c.549+299_549+300insAGGTTTAAAAAAAATTTTTTTTTTATTTCCTTTTTTTTTTTTTTTTT MANE Select	NP_000354.4:n.549+299_549+300insAGGTTTAAAAAAAATTTTTTTTTTATTTC...