Canonical Allele Identifier: CA2343273722
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154053C= , CM000681.2:g.55154053C= GRCh38
NC_000019.9:g.55665421C= , CM000681.1:g.55665421C= GRCh37
NC_000019.8:g.60357233C= NCBI36
NG_007866.2:g.8680G= , LRG_432:g.8680G=
NG_011829.2:g.186G=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.526G= MANE Select ENSP00000341838.5:p.Val176=
ENST00000665070.1:c.559G= ENSP00000499482.1:p.Val187=
ENST00000344887.9:c.526G= ENSP00000341838.5:p.Val176=
ENST00000585806.5:n.525G=
ENST00000588882.1:c.451G= ENSP00000466729.1:p.Val151=
ENST00000589864.1:n.354G=
NM_000363.4:c.526G= , LRG_432t1:c.526G= NP_000354.4:p.Val176=
NM_000363.5:c.526G= MANE Select NP_000354.4:p.Val176=