Canonical Allele Identifier: CA10581187
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 235062
dbSNP Id: rs876661394

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154056G>A , CM000681.2:g.55154056G>A GRCh38
NC_000019.9:g.55665424G>A , CM000681.1:g.55665424G>A GRCh37
NC_000019.8:g.60357236G>A NCBI36
NG_007866.2:g.8677C>T , LRG_432:g.8677C>T
NG_011829.2:g.183C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.523C>T MANE Select ENSP00000341838.5:p.Gln175Ter
ENST00000665070.1:c.556C>T ENSP00000499482.1:p.Gln186Ter
ENST00000344887.9:c.523C>T ENSP00000341838.5:p.Gln175Ter
ENST00000585806.5:n.522C>T
ENST00000588882.1:c.448C>T ENSP00000466729.1:p.Gln150Ter
ENST00000589864.1:n.351C>T
NM_000363.4:c.523C>T , LRG_432t1:c.523C>T NP_000354.4:p.Gln175Ter
NM_000363.5:c.523C>T MANE Select NP_000354.4:p.Gln175Ter