Canonical Allele Identifier: CA407440976
Gene: TNNI3 HGNC NCBI

Linked Data

COSMIC: COSM440340

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154763T>C , CM000681.2:g.55154763T>C GRCh38
NC_000019.9:g.55666131T>C , CM000681.1:g.55666131T>C GRCh37
NC_000019.8:g.60357943T>C NCBI36
NG_007866.2:g.7970A>G , LRG_432:g.7970A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.350A>G MANE Select ENSP00000341838.5:p.Lys117Arg
ENST00000665070.1:c.350A>G ENSP00000499482.1:p.Lys117Arg
ENST00000344887.9:c.350A>G ENSP00000341838.5:p.Lys117Arg
ENST00000585806.5:n.349A>G
ENST00000586669.5:n.358A>G
ENST00000587176.5:n.534A>G
ENST00000587871.1:c.969A>G
ENST00000588882.1:c.275A>G ENSP00000466729.1:p.Lys92Arg
ENST00000590463.1:n.522A>G
NM_000363.4:c.350A>G , LRG_432t1:c.350A>G NP_000354.4:p.Lys117Arg
NM_000363.5:c.350A>G MANE Select NP_000354.4:p.Lys117Arg