Canonical Allele Identifier: CA2343273797
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154178T= , CM000681.2:g.55154178T= GRCh38
NC_000019.9:g.55665546T= , CM000681.1:g.55665546T= GRCh37
NC_000019.8:g.60357358T= NCBI36
NG_007866.2:g.8555A= , LRG_432:g.8555A=
NG_011829.2:g.61A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.401A= MANE Select ENSP00000341838.5:p.Asp134=
ENST00000665070.1:c.434A= ENSP00000499482.1:p.Asp145=
ENST00000344887.9:c.401A= ENSP00000341838.5:p.Asp134=
ENST00000585806.5:n.400A=
ENST00000586669.5:n.409A=
ENST00000588882.1:c.326A= ENSP00000466729.1:p.Asp109=
ENST00000589864.1:n.229A=
NM_000363.4:c.401A= , LRG_432t1:c.401A= NP_000354.4:p.Asp134=
NM_000363.5:c.401A= MANE Select NP_000354.4:p.Asp134=