Canonical Allele Identifier: CA031558

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201363296_201363297del , CM000663.2:g.201363296_201363297del	GRCh38
NC_000001.10:g.201332424_201332425del , CM000663.1:g.201332424_201332425del	GRCh37
NC_000001.9:g.199599047_199599048del	NCBI36
NG_007556.1:g.19381_19382del

Transcript Alleles

HGVS	Amino-acid change
ENST00000455702.7:c.584_585del	ENSP00000402238.3:p.Lys195ThrfsTer14
ENST00000367318.10:c.569_570del	ENSP00000356287.5:p.Lys190ThrfsTer14
ENST00000367322.6:c.566_567del	ENSP00000356291.2:p.Lys189AsnfsTer11
ENST00000412633.3:c.569_570del	ENSP00000408731.2:p.Lys190AsnfsTer11
ENST00000422165.6:c.599_600del	ENSP00000395163.2:p.Lys200AsnfsTer11
ENST00000438742.6:c.551_552del	ENSP00000414036.2:p.Lys184SerfsTer13
ENST00000455702.6:c.584_585del	ENSP00000402238.2:p.Lys195ThrfsTer14
ENST00000651504.1:n.1063_1064del
ENST00000656932.1:c.599_600del MANE Select	ENSP00000499593.1:p.Lys200ThrfsTer14
ENST00000658476.1:c.569_570del	ENSP00000499741.1:p.Lys190ThrfsTer14
ENST00000660295.1:c.569_570del	ENSP00000499418.1:p.Lys190ThrfsTer14
ENST00000662159.1:c.163-1298_163-1297del	ENSP00000499796.1:n.163-1298_163-1297del
ENST00000663843.1:c.*499_*500del	ENSP00000499590.1:n.*499_*500del
ENST00000666449.1:c.569_570del	ENSP00000499667.1:p.Lys190ThrfsTer14
ENST00000236918.11:c.599_600del	ENSP00000236918.8:p.Lys200ThrfsTer14
ENST00000360372.8:c.479_480del	ENSP00000353535.5:p.Lys160AsnfsTer11
ENST00000367315.6:c.575_576del	ENSP00000356284.3:p.Lys192ThrfsTer15
ENST00000367317.8:c.554_555del	ENSP00000356286.5:p.Lys185SerfsTer13
ENST00000367318.9:c.569_570del	ENSP00000356287.5:p.Lys190ThrfsTer14
ENST00000367320.6:c.479_480del	ENSP00000356289.2:p.Lys160AsnfsTer11
ENST00000367322.5:c.569_570del	ENSP00000356291.1:p.Lys190AsnfsTer11
ENST00000421663.6:c.392_393del	ENSP00000404134.3:p.Lys131AsnfsTer11
ENST00000438742.5:c.554_555del	ENSP00000414036.1:p.Lys185SerfsTer13
ENST00000458432.6:c.392_393del	ENSP00000387874.3:p.Lys131AsnfsTer11
ENST00000460780.5:n.892_893del
ENST00000476888.5:n.54_55del
ENST00000491504.5:n.1808_1809del
ENST00000509001.5:c.569_570del	ENSP00000422031.1:p.Lys190ThrfsTer14
ENST00000515042.5:n.495_496del
NM_000364.3:c.599_600del	NP_000355.2:p.Lys200AsnfsTer11
NM_001001430.2:c.569_570del	NP_001001430.1:p.Lys190ThrfsTer14
NM_001001431.2:c.569_570del	NP_001001431.1:p.Lys190AsnfsTer11
NM_001001432.2:c.554_555del	NP_001001432.1:p.Lys185SerfsTer13
NM_001276345.1:c.599_600del	NP_001263274.1:p.Lys200ThrfsTer14
NM_001276346.1:c.479_480del	NP_001263275.1:p.Lys160AsnfsTer11
NM_001276347.1:c.569_570del	NP_001263276.1:p.Lys190ThrfsTer14
XM_006711508.2:c.569_570del	XP_006711571.1:p.Lys190ThrfsTer14
XM_006711509.2:c.566_567del	XP_006711572.1:p.Lys189ThrfsTer14
XM_011509938.1:c.599_600del	XP_011508240.1:p.Lys200ThrfsTer14
XM_011509939.1:c.596_597del	XP_011508241.1:p.Lys199ThrfsTer14
XM_011509940.1:c.599_600del	XP_011508242.1:p.Lys200SerfsTer13
XM_011509941.1:c.596_597del	XP_011508243.1:p.Lys199SerfsTer13
XM_011509942.1:c.554_555del	XP_011508244.1:p.Lys185ThrfsTer14
XM_011509943.1:c.554_555del	XP_011508245.1:p.Lys185ThrfsTer14
XM_011509944.1:c.551_552del	XP_011508246.1:p.Lys184ThrfsTer14
XM_011509946.1:c.392_393del	XP_011508248.1:p.Lys131ThrfsTer14
XM_006711508.3:c.569_570del	XP_006711571.1:p.Lys190ThrfsTer14
XM_006711509.3:c.566_567del	XP_006711572.1:p.Lys189ThrfsTer14
XM_011509938.2:c.599_600del	XP_011508240.1:p.Lys200ThrfsTer14
XM_011509940.2:c.599_600del	XP_011508242.1:p.Lys200SerfsTer13
XM_011509941.2:c.596_597del	XP_011508243.1:p.Lys199SerfsTer13
XM_011509942.2:c.554_555del	XP_011508244.1:p.Lys185ThrfsTer14
XM_011509943.2:c.554_555del	XP_011508245.1:p.Lys185ThrfsTer14
XM_011509944.2:c.551_552del	XP_011508246.1:p.Lys184ThrfsTer14
XM_017002216.2:c.569_570del	XP_016857705.1:p.Lys190SerfsTer13
XM_017002217.1:c.569_570del	XP_016857706.1:p.Lys190AsnfsTer11
XM_024449450.1:c.599_600del	XP_024305218.1:p.Lys200ThrfsTer14
XM_024449454.1:c.566_567del	XP_024305222.1:p.Lys189ThrfsTer14
XM_024449455.1:c.569_570del	XP_024305223.1:p.Lys190SerfsTer13
NM_000364.4:c.599_600del	NP_000355.2:p.Lys200AsnfsTer11
NM_001001430.3:c.569_570del	NP_001001430.1:p.Lys190ThrfsTer14
NM_001001431.3:c.569_570del	NP_001001431.1:p.Lys190AsnfsTer11
NM_001001432.3:c.554_555del	NP_001001432.1:p.Lys185SerfsTer13
NM_001276345.2:c.599_600del MANE Select	NP_001263274.1:p.Lys200ThrfsTer14
NM_001276346.2:c.479_480del	NP_001263275.1:p.Lys160AsnfsTer11
NM_001276347.2:c.569_570del	NP_001263276.1:p.Lys190ThrfsTer14