Canonical Allele Identifier: CA2343275990
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157646G= , CM000681.2:g.55157646G= GRCh38
NC_000019.9:g.55669014G= , CM000681.1:g.55669014G= GRCh37
NC_000019.8:g.60360826G= NCBI36
NG_007866.2:g.5087C= , LRG_432:g.5087C=
NG_032759.1:g.14077C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.-57C= MANE Select ENSP00000341838.5:n.-57C=
ENST00000665070.1:c.-57C= ENSP00000499482.1:n.-57C=
ENST00000344887.9:c.-57C= ENSP00000341838.5:n.-57C=
ENST00000586446.1:n.87C=
ENST00000587176.5:n.128C=
ENST00000587871.1:c.564C=
ENST00000590463.1:n.71C=
NM_000363.4:c.-57C= , LRG_432t1:c.-57C= NP_000354.4:n.-57C=
NM_000363.5:c.-57C= MANE Select NP_000354.4:n.-57C=