Canonical Allele Identifier: CA2576892639
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153999A>T , CM000681.2:g.55153999A>T GRCh38
NC_000019.9:g.55665367A>T , CM000681.1:g.55665367A>T GRCh37
NC_000019.8:g.60357179A>T NCBI36
NG_007866.2:g.8734T>A , LRG_432:g.8734T>A
NG_011829.2:g.240T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+31T>A MANE Select ENSP00000341838.5:n.549+31T>A
ENST00000665070.1:c.582+31T>A ENSP00000499482.1:n.582+31T>A
ENST00000344887.9:c.549+31T>A ENSP00000341838.5:n.549+31T>A
ENST00000585806.5:n.548+31T>A
ENST00000588882.1:c.474+31T>A ENSP00000466729.1:n.474+31T>A
ENST00000589864.1:n.377+31T>A
NM_000363.4:c.549+31T>A , LRG_432t1:c.549+31T>A NP_000354.4:n.549+31T>A
NM_000363.5:c.549+31T>A MANE Select NP_000354.4:n.549+31T>A