Canonical Allele Identifier: CA407440288
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154062G>C , CM000681.2:g.55154062G>C GRCh38
NC_000019.9:g.55665430G>C , CM000681.1:g.55665430G>C GRCh37
NC_000019.8:g.60357242G>C NCBI36
NG_007866.2:g.8671C>G , LRG_432:g.8671C>G
NG_011829.2:g.177C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.517C>G MANE Select ENSP00000341838.5:p.Leu173Val
ENST00000665070.1:c.550C>G ENSP00000499482.1:p.Leu184Val
ENST00000344887.9:c.517C>G ENSP00000341838.5:p.Leu173Val
ENST00000585806.5:n.516C>G
ENST00000588882.1:c.442C>G ENSP00000466729.1:p.Leu148Val
ENST00000589864.1:n.345C>G
NM_000363.4:c.517C>G , LRG_432t1:c.517C>G NP_000354.4:p.Leu173Val
NM_000363.5:c.517C>G MANE Select NP_000354.4:p.Leu173Val