Canonical Allele Identifier: CA310148831

Gene: TNNI3

Linked Data

• dbSNP Id: rs35173650
• MyVariant Identifiers: chr19:g.55666144_55666145insA (hg19) ; chr19:g.55154776_55154777insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154776_55154777insA , CM000681.2:g.55154776_55154777insA	GRCh38
NC_000019.9:g.55666144_55666145insA , CM000681.1:g.55666144_55666145insA	GRCh37
NC_000019.8:g.60357956_60357957insA	NCBI36
NG_007866.2:g.7956_7957insT , LRG_432:g.7956_7957insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.336_337insT MANE Select	ENSP00000341838.5:p.Asp113Ter
ENST00000665070.1:c.336_337insT	ENSP00000499482.1:p.Asp113Ter
ENST00000344887.9:c.336_337insT	ENSP00000341838.5:p.Asp113Ter
ENST00000585806.5:n.335_336insT
ENST00000586669.5:n.344_345insT
ENST00000587176.5:n.520_521insT
ENST00000587871.1:c.955_956insT
ENST00000588882.1:c.261_262insT	ENSP00000466729.1:p.Asp88Ter
ENST00000590463.1:n.508_509insT
NM_000363.4:c.336_337insT , LRG_432t1:c.336_337insT	NP_000354.4:p.Asp113Ter
NM_000363.5:c.336_337insT MANE Select	NP_000354.4:p.Asp113Ter