Canonical Allele Identifier: CA2343275992
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157648T= , CM000681.2:g.55157648T= GRCh38
NC_000019.9:g.55669016T= , CM000681.1:g.55669016T= GRCh37
NC_000019.8:g.60360828T= NCBI36
NG_007866.2:g.5085A= , LRG_432:g.5085A=
NG_032759.1:g.14075A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.-59A= MANE Select ENSP00000341838.5:n.-59A=
ENST00000665070.1:c.-59A= ENSP00000499482.1:n.-59A=
ENST00000344887.9:c.-59A= ENSP00000341838.5:n.-59A=
ENST00000586446.1:n.85A=
ENST00000587176.5:n.126A=
ENST00000587871.1:c.562A=
ENST00000590463.1:n.69A=
NM_000363.4:c.-59A= , LRG_432t1:c.-59A= NP_000354.4:n.-59A=
NM_000363.5:c.-59A= MANE Select NP_000354.4:n.-59A=