Canonical Allele Identifier: CA2343273785
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154158G= , CM000681.2:g.55154158G= GRCh38
NC_000019.9:g.55665526G= , CM000681.1:g.55665526G= GRCh37
NC_000019.8:g.60357338G= NCBI36
NG_007866.2:g.8575C= , LRG_432:g.8575C=
NG_011829.2:g.81C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.421C= MANE Select ENSP00000341838.5:p.Arg141=
ENST00000665070.1:c.454C= ENSP00000499482.1:p.Arg152=
ENST00000344887.9:c.421C= ENSP00000341838.5:p.Arg141=
ENST00000585806.5:n.420C=
ENST00000586669.5:n.429C=
ENST00000588882.1:c.346C= ENSP00000466729.1:p.Arg116=
ENST00000589864.1:n.249C=
NM_000363.4:c.421C= , LRG_432t1:c.421C= NP_000354.4:p.Arg141=
NM_000363.5:c.421C= MANE Select NP_000354.4:p.Arg141=