Canonical Allele Identifier: CA2343275179
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156303C= , CM000681.2:g.55156303C= GRCh38
NC_000019.9:g.55667671C= , CM000681.1:g.55667671C= GRCh37
NC_000019.8:g.60359483C= NCBI36
NG_007866.2:g.6430G= , LRG_432:g.6430G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.180G= MANE Select ENSP00000341838.5:p.Glu60=
ENST00000665070.1:c.180G= ENSP00000499482.1:p.Glu60=
ENST00000344887.9:c.180G= ENSP00000341838.5:p.Glu60=
ENST00000585806.5:n.179G=
ENST00000586669.5:n.188G=
ENST00000586858.1:c.143G= ENSP00000465258.1:p.Ser48=
ENST00000587176.5:n.364G=
ENST00000587871.1:c.799G=
ENST00000588882.1:c.105G= ENSP00000466729.1:p.Glu35=
ENST00000590463.1:n.352G=
NM_000363.4:c.180G= , LRG_432t1:c.180G= NP_000354.4:p.Glu60=
NM_000363.5:c.180G= MANE Select NP_000354.4:p.Glu60=