Canonical Allele Identifier: CA2343272842
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55152239T= , CM000681.2:g.55152239T= GRCh38
NC_000019.9:g.55663607T= , CM000681.1:g.55663607T= GRCh37
NC_000019.8:g.60355419T= NCBI36
NG_007866.2:g.10494A= , LRG_432:g.10494A=
NG_011829.2:g.2000A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.550-322A= MANE Select ENSP00000341838.5:n.550-322A=
ENST00000665070.1:c.583-322A= ENSP00000499482.1:n.583-322A=
ENST00000344887.9:c.550-322A= ENSP00000341838.5:n.550-322A=
ENST00000585806.5:n.549-322A=
ENST00000588882.1:c.475-322A= ENSP00000466729.1:n.475-322A=
ENST00000589864.1:n.378-322A=
NM_000363.4:c.550-322A= , LRG_432t1:c.550-322A= NP_000354.4:n.550-322A=
NM_000363.5:c.550-322A= MANE Select NP_000354.4:n.550-322A=
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