Canonical Allele Identifier: CA2343275176
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156296G= , CM000681.2:g.55156296G= GRCh38
NC_000019.9:g.55667664G= , CM000681.1:g.55667664G= GRCh37
NC_000019.8:g.60359476G= NCBI36
NG_007866.2:g.6437C= , LRG_432:g.6437C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.187C= MANE Select ENSP00000341838.5:p.Arg63=
ENST00000665070.1:c.187C= ENSP00000499482.1:p.Arg63=
ENST00000344887.9:c.187C= ENSP00000341838.5:p.Arg63=
ENST00000585806.5:n.186C=
ENST00000586669.5:n.195C=
ENST00000586858.1:c.150C= ENSP00000465258.1:p.Ser50=
ENST00000587176.5:n.371C=
ENST00000587871.1:c.806C=
ENST00000588882.1:c.112C= ENSP00000466729.1:p.Arg38=
ENST00000590463.1:n.359C=
NM_000363.4:c.187C= , LRG_432t1:c.187C= NP_000354.4:p.Arg63=
NM_000363.5:c.187C= MANE Select NP_000354.4:p.Arg63=