Canonical Allele Identifier: CA407441656
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156202T>C , CM000681.2:g.55156202T>C GRCh38
NC_000019.9:g.55667570T>C , CM000681.1:g.55667570T>C GRCh37
NC_000019.8:g.60359382T>C NCBI36
NG_007866.2:g.6531A>G , LRG_432:g.6531A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.281A>G MANE Select ENSP00000341838.5:p.Gln94Arg
ENST00000665070.1:c.281A>G ENSP00000499482.1:p.Gln94Arg
ENST00000344887.9:c.281A>G ENSP00000341838.5:p.Gln94Arg
ENST00000585806.5:n.280A>G
ENST00000586669.5:n.289A>G
ENST00000587176.5:n.465A>G
ENST00000587871.1:c.900A>G
ENST00000588882.1:c.206A>G ENSP00000466729.1:p.Gln69Arg
ENST00000590463.1:n.453A>G
NM_000363.4:c.281A>G , LRG_432t1:c.281A>G NP_000354.4:p.Gln94Arg
NM_000363.5:c.281A>G MANE Select NP_000354.4:p.Gln94Arg