Canonical Allele Identifier: CA730092684

Gene: TNNT2

Linked Data

• ClinVar Variation Id: 2501582
• ClinVar RCV Id: RCV003227377
• dbSNP Id: rs1425237593
• gnomAD v4: 1-201373207-TACTC-T
• MyVariant Identifiers: chr1:g.201342336_201342339del (hg19) ; chr1:g.201373208_201373211del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201373212_201373215del , CM000663.2:g.201373212_201373215del	GRCh38
NC_000001.10:g.201342340_201342343del , CM000663.1:g.201342340_201342343del	GRCh37
NC_000001.9:g.199608963_199608966del	NCBI36
NG_007556.1:g.9467_9470del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.41+3_41+6del
ENST00000367318.10:c.41+3_41+6del
ENST00000367322.6:c.41+3_41+6del
ENST00000412633.3:c.41+3_41+6del
ENST00000422165.6:c.41+3_41+6del
ENST00000438742.6:c.41+3_41+6del
ENST00000455702.6:c.41+3_41+6del
ENST00000656932.1:c.41+3_41+6del
ENST00000658476.1:c.41+3_41+6del
ENST00000660295.1:c.41+3_41+6del
ENST00000662159.1:c.41+3_41+6del
ENST00000663843.1:c.41+3_41+6del
ENST00000666449.1:c.41+3_41+6del
ENST00000236918.11:c.41+3_41+6del
ENST00000360372.8:c.41+3_41+6del
ENST00000367315.6:c.40_43del
ENST00000367317.8:c.41+3_41+6del
ENST00000367318.9:c.41+3_41+6del
ENST00000367320.6:c.41+3_41+6del
ENST00000367322.5:c.41+3_41+6del
ENST00000412633.2:c.41+3_41+6del
ENST00000421663.6:c.-113_-111+1del
ENST00000422165.5:c.41+3_41+6del
ENST00000438742.5:c.41+3_41+6del
ENST00000455702.5:c.41+3_41+6del
ENST00000458432.6:c.-165_-162del	ENSP00000387874.3:n.-165_-162del
ENST00000466570.5:n.105_108del
ENST00000472177.2:n.113+3_113+6del
ENST00000475686.5:n.55_58del
ENST00000491504.5:n.113+3_113+6del
ENST00000494095.5:n.2155+3_2155+6del
ENST00000509001.5:c.41+3_41+6del
NM_000364.3:c.41+3_41+6del
NM_001001430.2:c.41+3_41+6del
NM_001001431.2:c.41+3_41+6del
NM_001001432.2:c.41+3_41+6del
NM_001276345.1:c.41+3_41+6del
NM_001276346.1:c.41+3_41+6del
NM_001276347.1:c.41+3_41+6del
XM_006711508.2:c.41+3_41+6del
XM_006711509.2:c.41+3_41+6del
XM_011509938.1:c.41+3_41+6del
XM_011509939.1:c.41+3_41+6del
XM_011509940.1:c.41+3_41+6del
XM_011509941.1:c.41+3_41+6del
XM_011509942.1:c.41+3_41+6del
XM_011509943.1:c.41+3_41+6del
XM_011509944.1:c.41+3_41+6del
XM_011509945.1:c.41+3_41+6del
XM_011509946.1:c.-229_-226del	XP_011508248.1:n.-229_-226del
XM_006711508.3:c.41+3_41+6del
XM_006711509.3:c.41+3_41+6del
XM_011509938.2:c.41+3_41+6del
XM_011509940.2:c.41+3_41+6del
XM_011509941.2:c.41+3_41+6del
XM_011509942.2:c.41+3_41+6del
XM_011509943.2:c.41+3_41+6del
XM_011509944.2:c.41+3_41+6del
XM_017002216.2:c.41+3_41+6del
XM_017002217.1:c.41+3_41+6del
XM_024449450.1:c.41+3_41+6del
XM_024449454.1:c.41+3_41+6del
XM_024449455.1:c.41+3_41+6del
NM_000364.4:c.41+3_41+6del
NM_001001430.3:c.41+3_41+6del
NM_001001431.3:c.41+3_41+6del
NM_001001432.3:c.41+3_41+6del
NM_001276345.2:c.41+3_41+6del
NM_001276346.2:c.41+3_41+6del
NM_001276347.2:c.41+3_41+6del