Canonical Allele Identifier: CA633906535

Gene: TNNI3

Linked Data

• dbSNP Id: rs1469214340
• gnomAD v2: 19-55667515-GGCTGTACTGCTGAATTCCGGGACTAGAAACCTC-G
• gnomAD v3: 19-55156147-GGCTGTACTGCTGAATTCCGGGACTAGAAACCTC-G
• gnomAD v4: 19-55156147-GGCTGTACTGCTGAATTCCGGGACTAGAAACCTC-G
• MyVariant Identifiers: chr19:g.55667516_55667548del (hg19) ; chr19:g.55156148_55156180del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156150_55156182del , CM000681.2:g.55156150_55156182del	GRCh38
NC_000019.9:g.55667518_55667550del , CM000681.1:g.55667518_55667550del	GRCh37
NC_000019.8:g.60359330_60359362del	NCBI36
NG_007866.2:g.6553_6585del , LRG_432:g.6553_6585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.282+21_282+53del MANE Select	ENSP00000341838.5:n.282+21_282+53del
ENST00000665070.1:c.282+21_282+53del	ENSP00000499482.1:n.282+21_282+53del
ENST00000344887.9:c.282+21_282+53del	ENSP00000341838.5:n.282+21_282+53del
ENST00000585806.5:n.281+21_281+53del
ENST00000586669.5:n.290+21_290+53del
ENST00000587176.5:n.466+21_466+53del
ENST00000587871.1:c.901+21_901+53del
ENST00000588882.1:c.207+21_207+53del	ENSP00000466729.1:n.207+21_207+53del
ENST00000590463.1:n.454+21_454+53del
NM_000363.4:c.282+21_282+53del , LRG_432t1:c.282+21_282+53del	NP_000354.4:n.282+21_282+53del
NM_000363.5:c.282+21_282+53del MANE Select	NP_000354.4:n.282+21_282+53del