Canonical Allele Identifier: CA2343275980
Gene: TNNI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55157628G= , CM000681.2:g.55157628G= GRCh38
NC_000019.9:g.55668996G= , CM000681.1:g.55668996G= GRCh37
NC_000019.8:g.60360808G= NCBI36
NG_007866.2:g.5105C= , LRG_432:g.5105C=
NG_032759.1:g.14095C=

Transcript Alleles

HGVS Amino-acid change
ENST00000344887.10:c.-39C= MANE Select ENSP00000341838.5:n.-39C=
ENST00000665070.1:c.-39C= ENSP00000499482.1:n.-39C=
ENST00000344887.9:c.-39C= ENSP00000341838.5:n.-39C=
ENST00000586446.1:n.105C=
ENST00000587176.5:n.146C=
ENST00000587871.1:c.582C=
ENST00000590463.1:n.89C=
NM_000363.4:c.-39C= , LRG_432t1:c.-39C= NP_000354.4:n.-39C=
NM_000363.5:c.-39C= MANE Select NP_000354.4:n.-39C=