Canonical Allele Identifier: CA407441102
Gene: TNNI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55154798G>T , CM000681.2:g.55154798G>T GRCh38
NC_000019.9:g.55666166G>T , CM000681.1:g.55666166G>T GRCh37
NC_000019.8:g.60357978G>T NCBI36
NG_007866.2:g.7935C>A , LRG_432:g.7935C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344887.10:c.315C>A MANE Select ENSP00000341838.5:p.Asp105Glu
ENST00000665070.1:c.315C>A ENSP00000499482.1:p.Asp105Glu
ENST00000344887.9:c.315C>A ENSP00000341838.5:p.Asp105Glu
ENST00000585806.5:n.314C>A
ENST00000586669.5:n.323C>A
ENST00000587176.5:n.499C>A
ENST00000587871.1:c.934C>A
ENST00000588882.1:c.240C>A ENSP00000466729.1:p.Asp80Glu
ENST00000590463.1:n.487C>A
NM_000363.4:c.315C>A , LRG_432t1:c.315C>A NP_000354.4:p.Asp105Glu
NM_000363.5:c.315C>A MANE Select NP_000354.4:p.Asp105Glu