Canonical Allele Identifier: CA2343275178
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156299C= , CM000681.2:g.55156299C= GRCh38
NC_000019.9:g.55667667C= , CM000681.1:g.55667667C= GRCh37
NC_000019.8:g.60359479C= NCBI36
NG_007866.2:g.6434G= , LRG_432:g.6434G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.184G= MANE Select ENSP00000341838.5:p.Glu62=
ENST00000665070.1:c.184G= ENSP00000499482.1:p.Glu62=
ENST00000344887.9:c.184G= ENSP00000341838.5:p.Glu62=
ENST00000585806.5:n.183G=
ENST00000586669.5:n.192G=
ENST00000586858.1:c.147G= ENSP00000465258.1:p.Trp49=
ENST00000587176.5:n.368G=
ENST00000587871.1:c.803G=
ENST00000588882.1:c.109G= ENSP00000466729.1:p.Glu37=
ENST00000590463.1:n.356G=
NM_000363.4:c.184G= , LRG_432t1:c.184G= NP_000354.4:p.Glu62=
NM_000363.5:c.184G= MANE Select NP_000354.4:p.Glu62=