Canonical Allele Identifier: CA2695229176
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157092_55157093delinsAA , CM000681.2:g.55157092_55157093delinsAA GRCh38
NC_000019.9:g.55668460_55668461delinsAA , CM000681.1:g.55668460_55668461delinsAA GRCh37
NC_000019.8:g.60360272_60360273delinsAA NCBI36
NG_007866.2:g.5640_5641delinsTT , LRG_432:g.5640_5641delinsTT
NG_032759.1:g.14630_14631delinsTT

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.65_66delinsTT MANE Select ENSP00000341838.5:p.Arg22Leu
ENST00000665070.1:c.65_66delinsTT ENSP00000499482.1:p.Arg22Leu
ENST00000344887.9:c.65_66delinsTT ENSP00000341838.5:p.Arg22Leu
ENST00000586446.1:n.207_208delinsTT
ENST00000586669.5:n.73_74delinsTT
ENST00000587176.5:n.249_250delinsTT
ENST00000587871.1:c.684_685delinsTT
ENST00000590463.1:n.237_238delinsTT
NM_000363.4:c.65_66delinsTT , LRG_432t1:c.65_66delinsTT NP_000354.4:p.Arg22Leu
NM_000363.5:c.65_66delinsTT MANE Select NP_000354.4:p.Arg22Leu