Canonical Allele Identifier: CA633871319

Gene: TNNI3

Linked Data

• dbSNP Id: rs1181683730
• gnomAD v2: 19-55666311-AGAAGGG-A
• gnomAD v3: 19-55154943-AGAAGGG-A
• gnomAD v4: 19-55154943-AGAAGGG-A
• MyVariant Identifiers: chr19:g.55666312_55666317del (hg19) ; chr19:g.55154944_55154949del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154945_55154950del , CM000681.2:g.55154945_55154950del	GRCh38
NC_000019.9:g.55666313_55666318del , CM000681.1:g.55666313_55666318del	GRCh37
NC_000019.8:g.60358125_60358130del	NCBI36
NG_007866.2:g.7784_7789del , LRG_432:g.7784_7789del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.283-119_283-114del MANE Select	ENSP00000341838.5:n.283-119_283-114del
ENST00000665070.1:c.283-119_283-114del	ENSP00000499482.1:n.283-119_283-114del
ENST00000344887.9:c.283-119_283-114del	ENSP00000341838.5:n.283-119_283-114del
ENST00000585806.5:n.282-119_282-114del
ENST00000586669.5:n.291-119_291-114del
ENST00000587176.5:n.467-119_467-114del
ENST00000587871.1:c.902-119_902-114del
ENST00000588882.1:c.208-119_208-114del	ENSP00000466729.1:n.208-119_208-114del
ENST00000590463.1:n.455-119_455-114del
NM_000363.4:c.283-119_283-114del , LRG_432t1:c.283-119_283-114del	NP_000354.4:n.283-119_283-114del
NM_000363.5:c.283-119_283-114del MANE Select	NP_000354.4:n.283-119_283-114del