Canonical Allele Identifier: CA2343273772
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154139A= , CM000681.2:g.55154139A= GRCh38
NC_000019.9:g.55665507A= , CM000681.1:g.55665507A= GRCh37
NC_000019.8:g.60357319A= NCBI36
NG_007866.2:g.8594T= , LRG_432:g.8594T=
NG_011829.2:g.100T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.440T= MANE Select ENSP00000341838.5:p.Val147=
ENST00000665070.1:c.473T= ENSP00000499482.1:p.Val158=
ENST00000344887.9:c.440T= ENSP00000341838.5:p.Val147=
ENST00000585806.5:n.439T=
ENST00000586669.5:n.448T=
ENST00000588882.1:c.365T= ENSP00000466729.1:p.Val122=
ENST00000589864.1:n.268T=
NM_000363.4:c.440T= , LRG_432t1:c.440T= NP_000354.4:p.Val147=
NM_000363.5:c.440T= MANE Select NP_000354.4:p.Val147=