Canonical Allele Identifier: CA2343273652
Gene: TNNI3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55153923T= , CM000681.2:g.55153923T= GRCh38
NC_000019.9:g.55665291T= , CM000681.1:g.55665291T= GRCh37
NC_000019.8:g.60357103T= NCBI36
NG_007866.2:g.8810A= , LRG_432:g.8810A=
NG_011829.2:g.316A=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.549+107A= MANE Select ENSP00000341838.5:n.549+107A=
ENST00000665070.1:c.582+107A= ENSP00000499482.1:n.582+107A=
ENST00000344887.9:c.549+107A= ENSP00000341838.5:n.549+107A=
ENST00000585806.5:n.548+107A=
ENST00000588882.1:c.474+107A= ENSP00000466729.1:n.474+107A=
ENST00000589864.1:n.377+107A=
NM_000363.4:c.549+107A= , LRG_432t1:c.549+107A= NP_000354.4:n.549+107A=
NM_000363.5:c.549+107A= MANE Select NP_000354.4:n.549+107A=
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