Canonical Allele Identifier: CA2548978306
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156134A>T , CM000681.2:g.55156134A>T GRCh38
NC_000019.9:g.55667502A>T , CM000681.1:g.55667502A>T GRCh37
NC_000019.8:g.60359314A>T NCBI36
NG_007866.2:g.6599T>A , LRG_432:g.6599T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.282+67T>A MANE Select ENSP00000341838.5:n.282+67T>A
ENST00000665070.1:c.282+67T>A ENSP00000499482.1:n.282+67T>A
ENST00000344887.9:c.282+67T>A ENSP00000341838.5:n.282+67T>A
ENST00000585806.5:n.281+67T>A
ENST00000586669.5:n.290+67T>A
ENST00000587176.5:n.466+67T>A
ENST00000587871.1:c.901+67T>A
ENST00000588882.1:c.207+67T>A ENSP00000466729.1:n.207+67T>A
ENST00000590463.1:n.454+67T>A
NM_000363.4:c.282+67T>A , LRG_432t1:c.282+67T>A NP_000354.4:n.282+67T>A
NM_000363.5:c.282+67T>A MANE Select NP_000354.4:n.282+67T>A