Canonical Allele Identifier: CA407440373
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154100C>G , CM000681.2:g.55154100C>G GRCh38
NC_000019.9:g.55665468C>G , CM000681.1:g.55665468C>G GRCh37
NC_000019.8:g.60357280C>G NCBI36
NG_007866.2:g.8633G>C , LRG_432:g.8633G>C
NG_011829.2:g.139G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.479G>C MANE Select ENSP00000341838.5:p.Gly160Ala
ENST00000665070.1:c.512G>C ENSP00000499482.1:p.Gly171Ala
ENST00000344887.9:c.479G>C ENSP00000341838.5:p.Gly160Ala
ENST00000585806.5:n.478G>C
ENST00000588882.1:c.404G>C ENSP00000466729.1:p.Gly135Ala
ENST00000589864.1:n.307G>C
NM_000363.4:c.479G>C , LRG_432t1:c.479G>C NP_000354.4:p.Gly160Ala
NM_000363.5:c.479G>C MANE Select NP_000354.4:p.Gly160Ala