Canonical Allele Identifier: CA407440393
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154106A>C , CM000681.2:g.55154106A>C GRCh38
NC_000019.9:g.55665474A>C , CM000681.1:g.55665474A>C GRCh37
NC_000019.8:g.60357286A>C NCBI36
NG_007866.2:g.8627T>G , LRG_432:g.8627T>G
NG_011829.2:g.133T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.473T>G MANE Select ENSP00000341838.5:p.Leu158Arg
ENST00000665070.1:c.506T>G ENSP00000499482.1:p.Leu169Arg
ENST00000344887.9:c.473T>G ENSP00000341838.5:p.Leu158Arg
ENST00000585806.5:n.472T>G
ENST00000588882.1:c.398T>G ENSP00000466729.1:p.Leu133Arg
ENST00000589864.1:n.301T>G
NM_000363.4:c.473T>G , LRG_432t1:c.473T>G NP_000354.4:p.Leu158Arg
NM_000363.5:c.473T>G MANE Select NP_000354.4:p.Leu158Arg