Canonical Allele Identifier: CA2343273767
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154124T= , CM000681.2:g.55154124T= GRCh38
NC_000019.9:g.55665492T= , CM000681.1:g.55665492T= GRCh37
NC_000019.8:g.60357304T= NCBI36
NG_007866.2:g.8609A= , LRG_432:g.8609A=
NG_011829.2:g.115A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.455A= MANE Select ENSP00000341838.5:p.Asp152=
ENST00000665070.1:c.488A= ENSP00000499482.1:p.Asp163=
ENST00000344887.9:c.455A= ENSP00000341838.5:p.Asp152=
ENST00000585806.5:n.454A=
ENST00000586669.5:n.463A=
ENST00000588882.1:c.380A= ENSP00000466729.1:p.Asp127=
ENST00000589864.1:n.283A=
NM_000363.4:c.455A= , LRG_432t1:c.455A= NP_000354.4:p.Asp152=
NM_000363.5:c.455A= MANE Select NP_000354.4:p.Asp152=