Canonical Allele Identifier: CA2695229160
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154147_55154148delinsAT , CM000681.2:g.55154147_55154148delinsAT GRCh38
NC_000019.9:g.55665515_55665516delinsAT , CM000681.1:g.55665515_55665516delinsAT GRCh37
NC_000019.8:g.60357327_60357328delinsAT NCBI36
NG_007866.2:g.8585_8586delinsAT , LRG_432:g.8585_8586delinsAT
NG_011829.2:g.91_92delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.431_432delinsAT MANE Select ENSP00000341838.5:p.Leu144His
ENST00000665070.1:c.464_465delinsAT ENSP00000499482.1:p.Leu155His
ENST00000344887.9:c.431_432delinsAT ENSP00000341838.5:p.Leu144His
ENST00000585806.5:n.430_431delinsAT
ENST00000586669.5:n.439_440delinsAT
ENST00000588882.1:c.356_357delinsAT ENSP00000466729.1:p.Leu119His
ENST00000589864.1:n.259_260delinsAT
NM_000363.4:c.431_432delinsAT , LRG_432t1:c.431_432delinsAT NP_000354.4:p.Leu144His
NM_000363.5:c.431_432delinsAT MANE Select NP_000354.4:p.Leu144His