Canonical Allele Identifier: CA915941976

Gene: TNNT2

Linked Data

• ClinVar Variation Id: 684850
• ClinVar RCV Id: RCV000845505
• dbSNP Id: rs1571627587

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201365270_201365275del , CM000663.2:g.201365270_201365275del	GRCh38
NC_000001.10:g.201334398_201334403del , CM000663.1:g.201334398_201334403del	GRCh37
NC_000001.9:g.199601021_199601026del	NCBI36
NG_007556.1:g.17404_17409del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.313_318del	ENSP00000402238.3:p.Asn105_Glu106del
ENST00000367318.10:c.298_303del	ENSP00000356287.5:p.Asn100_Glu101del
ENST00000367322.6:c.295_300del	ENSP00000356291.2:p.Asn99_Glu100del
ENST00000412633.3:c.298_303del	ENSP00000408731.2:p.Asn100_Glu101del
ENST00000422165.6:c.328_333del	ENSP00000395163.2:p.Asn110_Glu111del
ENST00000438742.6:c.280_285del	ENSP00000414036.2:p.Asn94_Glu95del
ENST00000455702.6:c.313_318del	ENSP00000402238.2:p.Asn105_Glu106del
ENST00000651504.1:n.792_797del
ENST00000656932.1:c.328_333del MANE Select	ENSP00000499593.1:p.Asn110_Glu111del
ENST00000658476.1:c.298_303del	ENSP00000499741.1:p.Asn100_Glu101del
ENST00000660295.1:c.298_303del	ENSP00000499418.1:p.Asn100_Glu101del
ENST00000662159.1:c.162+2504_162+2509del	ENSP00000499796.1:n.162+2504_162+2509del
ENST00000663843.1:c.*228_*233del	ENSP00000499590.1:n.*228_*233del
ENST00000666449.1:c.298_303del	ENSP00000499667.1:p.Asn100_Glu101del
ENST00000236918.11:c.328_333del	ENSP00000236918.8:p.Asn110_Glu111del
ENST00000360372.8:c.291+336_291+341del	ENSP00000353535.5:n.291+336_291+341del
ENST00000367315.6:c.304_309del	ENSP00000356284.3:p.Asn102_Glu103del
ENST00000367317.8:c.283_288del	ENSP00000356286.5:p.Asn95_Glu96del
ENST00000367318.9:c.298_303del	ENSP00000356287.5:p.Asn100_Glu101del
ENST00000367320.6:c.291+336_291+341del	ENSP00000356289.2:n.291+336_291+341del
ENST00000367322.5:c.298_303del	ENSP00000356291.1:p.Asn100_Glu101del
ENST00000421663.6:c.121_126del	ENSP00000404134.3:p.Asn41_Glu42del
ENST00000422165.5:c.313_318del	ENSP00000395163.1:p.Asn105_Glu106del
ENST00000438742.5:c.283_288del	ENSP00000414036.1:p.Asn95_Glu96del
ENST00000455702.5:c.328_333del	ENSP00000402238.1:p.Asn110_Glu111del
ENST00000458432.6:c.121_126del	ENSP00000387874.3:p.Asn41_Glu42del
ENST00000466570.5:n.554_559del
ENST00000491504.5:n.1537_1542del
ENST00000503459.1:n.167_172del
ENST00000509001.5:c.298_303del	ENSP00000422031.1:p.Asn100_Glu101del
ENST00000515042.5:n.224_229del
NM_000364.3:c.328_333del	NP_000355.2:p.Asn110_Glu111del
NM_001001430.2:c.298_303del	NP_001001430.1:p.Asn100_Glu101del
NM_001001431.2:c.298_303del	NP_001001431.1:p.Asn100_Glu101del
NM_001001432.2:c.283_288del	NP_001001432.1:p.Asn95_Glu96del
NM_001276345.1:c.328_333del	NP_001263274.1:p.Asn110_Glu111del
NM_001276346.1:c.291+336_291+341del	NP_001263275.1:n.291+336_291+341del
NM_001276347.1:c.298_303del	NP_001263276.1:p.Asn100_Glu101del
XM_006711508.2:c.298_303del	XP_006711571.1:p.Asn100_Glu101del
XM_006711509.2:c.295_300del	XP_006711572.1:p.Asn99_Glu100del
XM_011509938.1:c.328_333del	XP_011508240.1:p.Asn110_Glu111del
XM_011509939.1:c.325_330del	XP_011508241.1:p.Asn109_Glu110del
XM_011509940.1:c.328_333del	XP_011508242.1:p.Asn110_Glu111del
XM_011509941.1:c.325_330del	XP_011508243.1:p.Asn109_Glu110del
XM_011509942.1:c.283_288del	XP_011508244.1:p.Asn95_Glu96del
XM_011509943.1:c.283_288del	XP_011508245.1:p.Asn95_Glu96del
XM_011509944.1:c.280_285del	XP_011508246.1:p.Asn94_Glu95del
XM_011509945.1:c.328_333del	XP_011508247.1:p.Asn110_Glu111del
XM_011509946.1:c.121_126del	XP_011508248.1:p.Asn41_Glu42del
XM_006711508.3:c.298_303del	XP_006711571.1:p.Asn100_Glu101del
XM_006711509.3:c.295_300del	XP_006711572.1:p.Asn99_Glu100del
XM_011509938.2:c.328_333del	XP_011508240.1:p.Asn110_Glu111del
XM_011509940.2:c.328_333del	XP_011508242.1:p.Asn110_Glu111del
XM_011509941.2:c.325_330del	XP_011508243.1:p.Asn109_Glu110del
XM_011509942.2:c.283_288del	XP_011508244.1:p.Asn95_Glu96del
XM_011509943.2:c.283_288del	XP_011508245.1:p.Asn95_Glu96del
XM_011509944.2:c.280_285del	XP_011508246.1:p.Asn94_Glu95del
XM_017002216.2:c.298_303del	XP_016857705.1:p.Asn100_Glu101del
XM_017002217.1:c.298_303del	XP_016857706.1:p.Asn100_Glu101del
XM_024449450.1:c.328_333del	XP_024305218.1:p.Asn110_Glu111del
XM_024449454.1:c.295_300del	XP_024305222.1:p.Asn99_Glu100del
XM_024449455.1:c.298_303del	XP_024305223.1:p.Asn100_Glu101del
NM_000364.4:c.328_333del	NP_000355.2:p.Asn110_Glu111del
NM_001001430.3:c.298_303del	NP_001001430.1:p.Asn100_Glu101del
NM_001001431.3:c.298_303del	NP_001001431.1:p.Asn100_Glu101del
NM_001001432.3:c.283_288del	NP_001001432.1:p.Asn95_Glu96del
NM_001276345.2:c.328_333del MANE Select	NP_001263274.1:p.Asn110_Glu111del
NM_001276346.2:c.291+336_291+341del	NP_001263275.1:n.291+336_291+341del
NM_001276347.2:c.298_303del	NP_001263276.1:p.Asn100_Glu101del