Canonical Allele Identifier: CA407440274
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2708720
ClinVar RCV Id: RCV003586769

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154055T>C , CM000681.2:g.55154055T>C GRCh38
NC_000019.9:g.55665423T>C , CM000681.1:g.55665423T>C GRCh37
NC_000019.8:g.60357235T>C NCBI36
NG_007866.2:g.8678A>G , LRG_432:g.8678A>G
NG_011829.2:g.184A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.524A>G MANE Select ENSP00000341838.5:p.Gln175Arg
ENST00000665070.1:c.557A>G ENSP00000499482.1:p.Gln186Arg
ENST00000344887.9:c.524A>G ENSP00000341838.5:p.Gln175Arg
ENST00000585806.5:n.523A>G
ENST00000588882.1:c.449A>G ENSP00000466729.1:p.Gln150Arg
ENST00000589864.1:n.352A>G
NM_000363.4:c.524A>G , LRG_432t1:c.524A>G NP_000354.4:p.Gln175Arg
NM_000363.5:c.524A>G MANE Select NP_000354.4:p.Gln175Arg