Canonical Allele Identifier: CA021835
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 12425
dbSNP Id: rs104894730

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154047T>C , CM000681.2:g.55154047T>C GRCh38
NC_000019.9:g.55665415T>C , CM000681.1:g.55665415T>C GRCh37
NC_000019.8:g.60357227T>C NCBI36
NG_007866.2:g.8686A>G , LRG_432:g.8686A>G
NG_011829.2:g.192A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.532A>G MANE Select ENSP00000341838.5:p.Lys178Glu
ENST00000665070.1:c.565A>G ENSP00000499482.1:p.Lys189Glu
ENST00000344887.9:c.532A>G ENSP00000341838.5:p.Lys178Glu
ENST00000585806.5:n.531A>G
ENST00000588882.1:c.457A>G ENSP00000466729.1:p.Lys153Glu
ENST00000589864.1:n.360A>G
NM_000363.4:c.532A>G , LRG_432t1:c.532A>G NP_000354.4:p.Lys178Glu
NM_000363.5:c.532A>G MANE Select NP_000354.4:p.Lys178Glu