Canonical Allele Identifier: CA2587243161
Gene: TNNI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2807748
ClinVar RCV Id: RCV003749405

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151923G>A , CM000681.2:g.55151923G>A GRCh38
NC_000019.9:g.55663291G>A , CM000681.1:g.55663291G>A GRCh37
NC_000019.8:g.60355103G>A NCBI36
NG_007866.2:g.10810C>T , LRG_432:g.10810C>T
NG_011829.2:g.2316C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.550-6C>T MANE Select ENSP00000341838.5:n.550-6C>T
ENST00000665070.1:c.583-6C>T ENSP00000499482.1:n.583-6C>T
ENST00000344887.9:c.550-6C>T ENSP00000341838.5:n.550-6C>T
ENST00000585806.5:n.549-6C>T
ENST00000588882.1:c.475-6C>T ENSP00000466729.1:n.475-6C>T
ENST00000589864.1:n.378-6C>T
NM_000363.4:c.550-6C>T , LRG_432t1:c.550-6C>T NP_000354.4:n.550-6C>T
NM_000363.5:c.550-6C>T MANE Select NP_000354.4:n.550-6C>T