Canonical Allele Identifier: CA407441003
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs2147283683

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154770C>T , CM000681.2:g.55154770C>T GRCh38
NC_000019.9:g.55666138C>T , CM000681.1:g.55666138C>T GRCh37
NC_000019.8:g.60357950C>T NCBI36
NG_007866.2:g.7963G>A , LRG_432:g.7963G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.343G>A MANE Select ENSP00000341838.5:p.Glu115Lys
ENST00000665070.1:c.343G>A ENSP00000499482.1:p.Glu115Lys
ENST00000344887.9:c.343G>A ENSP00000341838.5:p.Glu115Lys
ENST00000585806.5:n.342G>A
ENST00000586669.5:n.351G>A
ENST00000587176.5:n.527G>A
ENST00000587871.1:c.962G>A
ENST00000588882.1:c.268G>A ENSP00000466729.1:p.Glu90Lys
ENST00000590463.1:n.515G>A
NM_000363.4:c.343G>A , LRG_432t1:c.343G>A NP_000354.4:p.Glu115Lys
NM_000363.5:c.343G>A MANE Select NP_000354.4:p.Glu115Lys