Canonical Allele Identifier: CA2343272830
Gene: TNNI3 HGNC NCBI

Linked Data

dbSNP Id: rs2085699486

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55152221del , CM000681.2:g.55152221del GRCh38
NC_000019.9:g.55663589del , CM000681.1:g.55663589del GRCh37
NC_000019.8:g.60355401del NCBI36
NG_007866.2:g.10514del , LRG_432:g.10514del
NG_011829.2:g.2020del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.550-302del MANE Select ENSP00000341838.5:n.550-302del
ENST00000665070.1:c.583-302del ENSP00000499482.1:n.583-302del
ENST00000344887.9:c.550-302del ENSP00000341838.5:n.550-302del
ENST00000585806.5:n.549-302del
ENST00000588882.1:c.475-302del ENSP00000466729.1:n.475-302del
ENST00000589864.1:n.378-302del
NM_000363.4:c.550-302del , LRG_432t1:c.550-302del NP_000354.4:n.550-302del
NM_000363.5:c.550-302del MANE Select NP_000354.4:n.550-302del