Canonical Allele Identifier: CA2343275605
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55156999T= , CM000681.2:g.55156999T= GRCh38
NC_000019.9:g.55668367T= , CM000681.1:g.55668367T= GRCh37
NC_000019.8:g.60360179T= NCBI36
NG_007866.2:g.5734A= , LRG_432:g.5734A=
NG_032759.1:g.14724A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.108+51A= MANE Select ENSP00000341838.5:n.108+51A=
ENST00000665070.1:c.108+51A= ENSP00000499482.1:n.108+51A=
ENST00000344887.9:c.108+51A= ENSP00000341838.5:n.108+51A=
ENST00000586446.1:n.301A=
ENST00000586669.5:n.116+51A=
ENST00000587176.5:n.292+51A=
ENST00000587871.1:c.727+51A=
ENST00000590463.1:n.280+51A=
NM_000363.4:c.108+51A= , LRG_432t1:c.108+51A= NP_000354.4:n.108+51A=
NM_000363.5:c.108+51A= MANE Select NP_000354.4:n.108+51A=