Canonical Allele Identifier: CA2343275177
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156298T= , CM000681.2:g.55156298T= GRCh38
NC_000019.9:g.55667666T= , CM000681.1:g.55667666T= GRCh37
NC_000019.8:g.60359478T= NCBI36
NG_007866.2:g.6435A= , LRG_432:g.6435A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.185A= MANE Select ENSP00000341838.5:p.Glu62=
ENST00000665070.1:c.185A= ENSP00000499482.1:p.Glu62=
ENST00000344887.9:c.185A= ENSP00000341838.5:p.Glu62=
ENST00000585806.5:n.184A=
ENST00000586669.5:n.193A=
ENST00000586858.1:c.148A= ENSP00000465258.1:p.Ser50=
ENST00000587176.5:n.369A=
ENST00000587871.1:c.804A=
ENST00000588882.1:c.110A= ENSP00000466729.1:p.Glu37=
ENST00000590463.1:n.357A=
NM_000363.4:c.185A= , LRG_432t1:c.185A= NP_000354.4:p.Glu62=
NM_000363.5:c.185A= MANE Select NP_000354.4:p.Glu62=