Canonical Allele Identifier: CA2343274085
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154756G= , CM000681.2:g.55154756G= GRCh38
NC_000019.9:g.55666124G= , CM000681.1:g.55666124G= GRCh37
NC_000019.8:g.60357936G= NCBI36
NG_007866.2:g.7977C= , LRG_432:g.7977C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.357C= MANE Select ENSP00000341838.5:p.Thr119=
ENST00000665070.1:c.357C= ENSP00000499482.1:p.Thr119=
ENST00000344887.9:c.357C= ENSP00000341838.5:p.Thr119=
ENST00000585806.5:n.356C=
ENST00000586669.5:n.365C=
ENST00000587176.5:n.541C=
ENST00000588882.1:c.282C= ENSP00000466729.1:p.Thr94=
ENST00000590463.1:n.529C=
NM_000363.4:c.357C= , LRG_432t1:c.357C= NP_000354.4:p.Thr119=
NM_000363.5:c.357C= MANE Select NP_000354.4:p.Thr119=