Canonical Allele Identifier: CA2649787468

Gene: TNNT2

Linked Data

• gnomAD v4: 1-201363208-T-TGACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201363211_201363212insAGGAC , CM000663.2:g.201363211_201363212insAGGAC	GRCh38
NC_000001.10:g.201332339_201332340insAGGAC , CM000663.1:g.201332339_201332340insAGGAC	GRCh37
NC_000001.9:g.199598962_199598963insAGGAC	NCBI36
NG_007556.1:g.19469_19470insCTGTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000455702.7:c.585+87_585+88insCTGTC	ENSP00000402238.3:n.585+87_585+88insCTGTC
ENST00000367318.10:c.570+87_570+88insCTGTC	ENSP00000356287.5:n.570+87_570+88insCTGTC
ENST00000367322.6:c.567+87_567+88insCTGTC	ENSP00000356291.2:n.567+87_567+88insCTGTC
ENST00000412633.3:c.570+87_570+88insCTGTC	ENSP00000408731.2:n.570+87_570+88insCTGTC
ENST00000422165.6:c.600+87_600+88insCTGTC	ENSP00000395163.2:n.600+87_600+88insCTGTC
ENST00000438742.6:c.552+87_552+88insCTGTC	ENSP00000414036.2:n.552+87_552+88insCTGTC
ENST00000455702.6:c.585+87_585+88insCTGTC	ENSP00000402238.2:n.585+87_585+88insCTGTC
ENST00000651504.1:n.1064+87_1064+88insCTGTC
ENST00000656932.1:c.600+87_600+88insCTGTC MANE Select	ENSP00000499593.1:n.600+87_600+88insCTGTC
ENST00000658476.1:c.570+87_570+88insCTGTC	ENSP00000499741.1:n.570+87_570+88insCTGTC
ENST00000660295.1:c.570+87_570+88insCTGTC	ENSP00000499418.1:n.570+87_570+88insCTGTC
ENST00000662159.1:c.163-1210_163-1209insCTGTC	ENSP00000499796.1:n.163-1210_163-1209insCTGTC
ENST00000663843.1:c.*500+87_*500+88insCTGTC	ENSP00000499590.1:n.*500+87_*500+88insCTGTC
ENST00000666449.1:c.570+87_570+88insCTGTC	ENSP00000499667.1:n.570+87_570+88insCTGTC
ENST00000236918.11:c.600+87_600+88insCTGTC	ENSP00000236918.8:n.600+87_600+88insCTGTC
ENST00000360372.8:c.480+87_480+88insCTGTC	ENSP00000353535.5:n.480+87_480+88insCTGTC
ENST00000367315.6:c.576+87_576+88insCTGTC	ENSP00000356284.3:n.576+87_576+88insCTGTC
ENST00000367317.8:c.555+87_555+88insCTGTC	ENSP00000356286.5:n.555+87_555+88insCTGTC
ENST00000367318.9:c.570+87_570+88insCTGTC	ENSP00000356287.5:n.570+87_570+88insCTGTC
ENST00000367320.6:c.480+87_480+88insCTGTC	ENSP00000356289.2:n.480+87_480+88insCTGTC
ENST00000367322.5:c.570+87_570+88insCTGTC	ENSP00000356291.1:n.570+87_570+88insCTGTC
ENST00000421663.6:c.393+87_393+88insCTGTC	ENSP00000404134.3:n.393+87_393+88insCTGTC
ENST00000438742.5:c.555+87_555+88insCTGTC	ENSP00000414036.1:n.555+87_555+88insCTGTC
ENST00000458432.6:c.393+87_393+88insCTGTC	ENSP00000387874.3:n.393+87_393+88insCTGTC
ENST00000460780.5:n.893+87_893+88insCTGTC
ENST00000476888.5:n.55+87_55+88insCTGTC
ENST00000491504.5:n.1809+87_1809+88insCTGTC
ENST00000509001.5:c.570+87_570+88insCTGTC	ENSP00000422031.1:n.570+87_570+88insCTGTC
ENST00000515042.5:n.496+87_496+88insCTGTC
NM_000364.3:c.600+87_600+88insCTGTC	NP_000355.2:n.600+87_600+88insCTGTC
NM_001001430.2:c.570+87_570+88insCTGTC	NP_001001430.1:n.570+87_570+88insCTGTC
NM_001001431.2:c.570+87_570+88insCTGTC	NP_001001431.1:n.570+87_570+88insCTGTC
NM_001001432.2:c.555+87_555+88insCTGTC	NP_001001432.1:n.555+87_555+88insCTGTC
NM_001276345.1:c.600+87_600+88insCTGTC	NP_001263274.1:n.600+87_600+88insCTGTC
NM_001276346.1:c.480+87_480+88insCTGTC	NP_001263275.1:n.480+87_480+88insCTGTC
NM_001276347.1:c.570+87_570+88insCTGTC	NP_001263276.1:n.570+87_570+88insCTGTC
XM_006711508.2:c.570+87_570+88insCTGTC	XP_006711571.1:n.570+87_570+88insCTGTC
XM_006711509.2:c.567+87_567+88insCTGTC	XP_006711572.1:n.567+87_567+88insCTGTC
XM_011509938.1:c.600+87_600+88insCTGTC	XP_011508240.1:n.600+87_600+88insCTGTC
XM_011509939.1:c.597+87_597+88insCTGTC	XP_011508241.1:n.597+87_597+88insCTGTC
XM_011509940.1:c.600+87_600+88insCTGTC	XP_011508242.1:n.600+87_600+88insCTGTC
XM_011509941.1:c.597+87_597+88insCTGTC	XP_011508243.1:n.597+87_597+88insCTGTC
XM_011509942.1:c.555+87_555+88insCTGTC	XP_011508244.1:n.555+87_555+88insCTGTC
XM_011509943.1:c.555+87_555+88insCTGTC	XP_011508245.1:n.555+87_555+88insCTGTC
XM_011509944.1:c.552+87_552+88insCTGTC	XP_011508246.1:n.552+87_552+88insCTGTC
XM_011509946.1:c.393+87_393+88insCTGTC	XP_011508248.1:n.393+87_393+88insCTGTC
XM_006711508.3:c.570+87_570+88insCTGTC	XP_006711571.1:n.570+87_570+88insCTGTC
XM_006711509.3:c.567+87_567+88insCTGTC	XP_006711572.1:n.567+87_567+88insCTGTC
XM_011509938.2:c.600+87_600+88insCTGTC	XP_011508240.1:n.600+87_600+88insCTGTC
XM_011509940.2:c.600+87_600+88insCTGTC	XP_011508242.1:n.600+87_600+88insCTGTC
XM_011509941.2:c.597+87_597+88insCTGTC	XP_011508243.1:n.597+87_597+88insCTGTC
XM_011509942.2:c.555+87_555+88insCTGTC	XP_011508244.1:n.555+87_555+88insCTGTC
XM_011509943.2:c.555+87_555+88insCTGTC	XP_011508245.1:n.555+87_555+88insCTGTC
XM_011509944.2:c.552+87_552+88insCTGTC	XP_011508246.1:n.552+87_552+88insCTGTC
XM_017002216.2:c.570+87_570+88insCTGTC	XP_016857705.1:n.570+87_570+88insCTGTC
XM_017002217.1:c.570+87_570+88insCTGTC	XP_016857706.1:n.570+87_570+88insCTGTC
XM_024449450.1:c.600+87_600+88insCTGTC	XP_024305218.1:n.600+87_600+88insCTGTC
XM_024449454.1:c.567+87_567+88insCTGTC	XP_024305222.1:n.567+87_567+88insCTGTC
XM_024449455.1:c.570+87_570+88insCTGTC	XP_024305223.1:n.570+87_570+88insCTGTC
NM_000364.4:c.600+87_600+88insCTGTC	NP_000355.2:n.600+87_600+88insCTGTC
NM_001001430.3:c.570+87_570+88insCTGTC	NP_001001430.1:n.570+87_570+88insCTGTC
NM_001001431.3:c.570+87_570+88insCTGTC	NP_001001431.1:n.570+87_570+88insCTGTC
NM_001001432.3:c.555+87_555+88insCTGTC	NP_001001432.1:n.555+87_555+88insCTGTC
NM_001276345.2:c.600+87_600+88insCTGTC MANE Select	NP_001263274.1:n.600+87_600+88insCTGTC
NM_001276346.2:c.480+87_480+88insCTGTC	NP_001263275.1:n.480+87_480+88insCTGTC
NM_001276347.2:c.570+87_570+88insCTGTC	NP_001263276.1:n.570+87_570+88insCTGTC