Canonical Allele Identifier: CA2814880922
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55151774T>G , CM000681.2:g.55151774T>G GRCh38
NC_000019.9:g.55663142T>G , CM000681.1:g.55663142T>G GRCh37
NC_000019.8:g.60354954T>G NCBI36
NG_007866.2:g.10959A>C , LRG_432:g.10959A>C
NG_011829.2:g.2465A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.*60A>C MANE Select ENSP00000341838.5:n.*60A>C
ENST00000665070.1:c.*60A>C ENSP00000499482.1:n.*60A>C
ENST00000344887.9:c.*60A>C ENSP00000341838.5:n.*60A>C
ENST00000585806.5:n.692A>C
ENST00000588882.1:c.*60A>C ENSP00000466729.1:n.*60A>C
ENST00000589864.1:n.521A>C
NM_000363.4:c.*60A>C , LRG_432t1:c.*60A>C NP_000354.4:n.*60A>C
NM_000363.5:c.*60A>C MANE Select NP_000354.4:n.*60A>C
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