Canonical Allele Identifier: CA2343273796
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154177G= , CM000681.2:g.55154177G= GRCh38
NC_000019.9:g.55665545G= , CM000681.1:g.55665545G= GRCh37
NC_000019.8:g.60357357G= NCBI36
NG_007866.2:g.8556C= , LRG_432:g.8556C=
NG_011829.2:g.62C=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.402C= MANE Select ENSP00000341838.5:p.Asp134=
ENST00000665070.1:c.435C= ENSP00000499482.1:p.Asp145=
ENST00000344887.9:c.402C= ENSP00000341838.5:p.Asp134=
ENST00000585806.5:n.401C=
ENST00000586669.5:n.410C=
ENST00000588882.1:c.327C= ENSP00000466729.1:p.Asp109=
ENST00000589864.1:n.230C=
NM_000363.4:c.402C= , LRG_432t1:c.402C= NP_000354.4:p.Asp134=
NM_000363.5:c.402C= MANE Select NP_000354.4:p.Asp134=