Canonical Allele Identifier: CA2649787648

Gene: TNNT2

Linked Data

• gnomAD v4: 1-201363552-G-GTGCTGGCCCACAGGAGTCCACTGACTGAGAAATGACTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201363553_201363591dup , CM000663.2:g.201363553_201363591dup	GRCh38
NC_000001.10:g.201332681_201332719dup , CM000663.1:g.201332681_201332719dup	GRCh37
NC_000001.9:g.199599304_199599342dup	NCBI36
NG_007556.1:g.19087_19125dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.475-185_475-147dup	ENSP00000402238.3:n.475-185_475-147dup
ENST00000367318.10:c.460-185_460-147dup	ENSP00000356287.5:n.460-185_460-147dup
ENST00000367322.6:c.457-185_457-147dup	ENSP00000356291.2:n.457-185_457-147dup
ENST00000412633.3:c.460-185_460-147dup	ENSP00000408731.2:n.460-185_460-147dup
ENST00000422165.6:c.490-185_490-147dup	ENSP00000395163.2:n.490-185_490-147dup
ENST00000438742.6:c.442-185_442-147dup	ENSP00000414036.2:n.442-185_442-147dup
ENST00000455702.6:c.475-185_475-147dup	ENSP00000402238.2:n.475-185_475-147dup
ENST00000651504.1:n.954-185_954-147dup
ENST00000656932.1:c.490-185_490-147dup MANE Select	ENSP00000499593.1:n.490-185_490-147dup
ENST00000658476.1:c.460-185_460-147dup	ENSP00000499741.1:n.460-185_460-147dup
ENST00000660295.1:c.460-185_460-147dup	ENSP00000499418.1:n.460-185_460-147dup
ENST00000662159.1:c.163-1592_163-1554dup	ENSP00000499796.1:n.163-1592_163-1554dup
ENST00000663843.1:c.*390-185_*390-147dup	ENSP00000499590.1:n.*390-185_*390-147dup
ENST00000666449.1:c.460-185_460-147dup	ENSP00000499667.1:n.460-185_460-147dup
ENST00000236918.11:c.490-185_490-147dup	ENSP00000236918.8:n.490-185_490-147dup
ENST00000360372.8:c.370-185_370-147dup	ENSP00000353535.5:n.370-185_370-147dup
ENST00000367315.6:c.466-185_466-147dup	ENSP00000356284.3:n.466-185_466-147dup
ENST00000367317.8:c.445-185_445-147dup	ENSP00000356286.5:n.445-185_445-147dup
ENST00000367318.9:c.460-185_460-147dup	ENSP00000356287.5:n.460-185_460-147dup
ENST00000367320.6:c.370-185_370-147dup	ENSP00000356289.2:n.370-185_370-147dup
ENST00000367322.5:c.460-185_460-147dup	ENSP00000356291.1:n.460-185_460-147dup
ENST00000421663.6:c.283-185_283-147dup	ENSP00000404134.3:n.283-185_283-147dup
ENST00000438742.5:c.445-185_445-147dup	ENSP00000414036.1:n.445-185_445-147dup
ENST00000455702.5:c.490-185_490-147dup	ENSP00000402238.1:n.490-185_490-147dup
ENST00000458432.6:c.283-185_283-147dup	ENSP00000387874.3:n.283-185_283-147dup
ENST00000460780.5:n.598_636dup
ENST00000466570.5:n.716-185_716-147dup
ENST00000491504.5:n.1699-185_1699-147dup
ENST00000509001.5:c.460-185_460-147dup	ENSP00000422031.1:n.460-185_460-147dup
ENST00000515042.5:n.386-185_386-147dup
NM_000364.3:c.490-185_490-147dup	NP_000355.2:n.490-185_490-147dup
NM_001001430.2:c.460-185_460-147dup	NP_001001430.1:n.460-185_460-147dup
NM_001001431.2:c.460-185_460-147dup	NP_001001431.1:n.460-185_460-147dup
NM_001001432.2:c.445-185_445-147dup	NP_001001432.1:n.445-185_445-147dup
NM_001276345.1:c.490-185_490-147dup	NP_001263274.1:n.490-185_490-147dup
NM_001276346.1:c.370-185_370-147dup	NP_001263275.1:n.370-185_370-147dup
NM_001276347.1:c.460-185_460-147dup	NP_001263276.1:n.460-185_460-147dup
XM_006711508.2:c.460-185_460-147dup	XP_006711571.1:n.460-185_460-147dup
XM_006711509.2:c.457-185_457-147dup	XP_006711572.1:n.457-185_457-147dup
XM_011509938.1:c.490-185_490-147dup	XP_011508240.1:n.490-185_490-147dup
XM_011509939.1:c.487-185_487-147dup	XP_011508241.1:n.487-185_487-147dup
XM_011509940.1:c.490-185_490-147dup	XP_011508242.1:n.490-185_490-147dup
XM_011509941.1:c.487-185_487-147dup	XP_011508243.1:n.487-185_487-147dup
XM_011509942.1:c.445-185_445-147dup	XP_011508244.1:n.445-185_445-147dup
XM_011509943.1:c.445-185_445-147dup	XP_011508245.1:n.445-185_445-147dup
XM_011509944.1:c.442-185_442-147dup	XP_011508246.1:n.442-185_442-147dup
XM_011509945.1:c.639_677dup	XP_011508247.1:p.Gln225_His226insGlnGlnSerPheLeuSerGlnTrpThrP...
XM_011509946.1:c.283-185_283-147dup	XP_011508248.1:n.283-185_283-147dup
XM_006711508.3:c.460-185_460-147dup	XP_006711571.1:n.460-185_460-147dup
XM_006711509.3:c.457-185_457-147dup	XP_006711572.1:n.457-185_457-147dup
XM_011509938.2:c.490-185_490-147dup	XP_011508240.1:n.490-185_490-147dup
XM_011509940.2:c.490-185_490-147dup	XP_011508242.1:n.490-185_490-147dup
XM_011509941.2:c.487-185_487-147dup	XP_011508243.1:n.487-185_487-147dup
XM_011509942.2:c.445-185_445-147dup	XP_011508244.1:n.445-185_445-147dup
XM_011509943.2:c.445-185_445-147dup	XP_011508245.1:n.445-185_445-147dup
XM_011509944.2:c.442-185_442-147dup	XP_011508246.1:n.442-185_442-147dup
XM_017002216.2:c.460-185_460-147dup	XP_016857705.1:n.460-185_460-147dup
XM_017002217.1:c.460-185_460-147dup	XP_016857706.1:n.460-185_460-147dup
XM_024449450.1:c.490-185_490-147dup	XP_024305218.1:n.490-185_490-147dup
XM_024449454.1:c.457-185_457-147dup	XP_024305222.1:n.457-185_457-147dup
XM_024449455.1:c.460-185_460-147dup	XP_024305223.1:n.460-185_460-147dup
NM_000364.4:c.490-185_490-147dup	NP_000355.2:n.490-185_490-147dup
NM_001001430.3:c.460-185_460-147dup	NP_001001430.1:n.460-185_460-147dup
NM_001001431.3:c.460-185_460-147dup	NP_001001431.1:n.460-185_460-147dup
NM_001001432.3:c.445-185_445-147dup	NP_001001432.1:n.445-185_445-147dup
NM_001276345.2:c.490-185_490-147dup MANE Select	NP_001263274.1:n.490-185_490-147dup
NM_001276346.2:c.370-185_370-147dup	NP_001263275.1:n.370-185_370-147dup
NM_001276347.2:c.460-185_460-147dup	NP_001263276.1:n.460-185_460-147dup