Canonical Allele Identifier: CA155746

Gene: TNNT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1934874T>C , CM000673.2:g.1934874T>C	GRCh38
NC_000011.9:g.1956104T>C , CM000673.1:g.1956104T>C	GRCh37
NC_000011.8:g.1912680T>C	NCBI36
NG_013085.1:g.20306T>C
NG_013085.2:g.20306T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706488.1:c.630T>C	ENSP00000516410.1:p.Ile210=
ENST00000278317.11:c.636T>C MANE Select	ENSP00000278317.6:p.Ile212=
ENST00000381558.6:c.612T>C	ENSP00000370970.1:p.Ile204=
ENST00000639560.1:n.746T>C
ENST00000641119.1:c.630T>C	ENSP00000492914.1:p.Ile210=
ENST00000641225.1:c.432T>C	ENSP00000493372.1:p.Ile144=
ENST00000641787.1:c.612T>C	ENSP00000493331.1:p.Ile204=
ENST00000278317.10:c.636T>C	ENSP00000278317.6:p.Ile212=
ENST00000344578.8:c.597T>C	ENSP00000344870.4:p.Ile199=
ENST00000381557.6:c.594T>C	ENSP00000370969.2:p.Ile198=
ENST00000381558.5:c.612T>C	ENSP00000370970.1:p.Ile204=
ENST00000381563.8:c.645T>C	ENSP00000370975.4:p.Ile215=
ENST00000381579.7:c.612T>C	ENSP00000370991.3:p.Ile204=
ENST00000381589.7:c.630T>C	ENSP00000371001.3:p.Ile210=
ENST00000397301.5:c.669T>C	ENSP00000380468.1:p.Ile223=
ENST00000397304.6:c.579T>C	ENSP00000380471.2:p.Ile193=
ENST00000446240.1:c.579T>C	ENSP00000413203.1:p.Ile193=
ENST00000453458.5:c.579T>C	ENSP00000415614.1:p.Ile193=
ENST00000493234.1:n.406T>C
NM_001042780.2:c.612T>C	NP_001036245.1:p.Ile204=
NM_001042781.2:c.630T>C	NP_001036246.1:p.Ile210=
NM_001042782.2:c.612T>C	NP_001036247.1:p.Ile204=
NM_001297646.1:c.612T>C	NP_001284575.1:p.Ile204=
NM_006757.3:c.636T>C	NP_006748.1:p.Ile212=
XM_006718288.2:c.684T>C	XP_006718351.1:p.Ile228=
XM_006718290.2:c.669T>C	XP_006718353.1:p.Ile223=
XM_006718291.2:c.657T>C	XP_006718354.1:p.Ile219=
XM_006718292.2:c.648T>C	XP_006718355.1:p.Ile216=
XM_006718293.1:c.645T>C	XP_006718356.1:p.Ile215=
XM_006718294.2:c.645T>C	XP_006718357.1:p.Ile215=
XM_006718295.2:c.642T>C	XP_006718358.1:p.Ile214=
XM_006718296.2:c.633T>C	XP_006718359.1:p.Ile211=
XM_006718297.2:c.624T>C	XP_006718360.1:p.Ile208=
XM_006718298.2:c.618T>C	XP_006718361.1:p.Ile206=
XM_006718299.1:c.609T>C	XP_006718362.1:p.Ile203=
XM_006718300.2:c.597T>C	XP_006718363.1:p.Ile199=
XM_006718301.2:c.597T>C	XP_006718364.1:p.Ile199=
XM_006718302.2:c.579T>C	XP_006718365.1:p.Ile193=
XM_011520342.1:c.669T>C	XP_011518644.1:p.Ile223=
XM_011520343.1:c.669T>C	XP_011518645.1:p.Ile223=
NM_001363561.1:c.645T>C	NP_001350490.1:p.Ile215=
XM_006718288.3:c.684T>C	XP_006718351.1:p.Ile228=
XM_006718290.3:c.669T>C	XP_006718353.1:p.Ile223=
XM_006718294.3:c.645T>C	XP_006718357.1:p.Ile215=
XM_006718296.3:c.633T>C	XP_006718359.1:p.Ile211=
XM_006718299.2:c.609T>C	XP_006718362.1:p.Ile203=
XM_006718300.3:c.597T>C	XP_006718363.1:p.Ile199=
XM_006718302.3:c.579T>C	XP_006718365.1:p.Ile193=
XM_011520343.2:c.669T>C	XP_011518645.1:p.Ile223=
XM_017018205.1:c.630T>C	XP_016873694.1:p.Ile210=
XM_017018206.1:c.669T>C	XP_016873695.1:p.Ile223=
XM_017018207.1:c.657T>C	XP_016873696.1:p.Ile219=
XM_017018208.1:c.648T>C	XP_016873697.1:p.Ile216=
XM_017018209.1:c.633T>C	XP_016873698.1:p.Ile211=
XM_017018210.1:c.624T>C	XP_016873699.1:p.Ile208=
XM_017018211.1:c.618T>C	XP_016873700.1:p.Ile206=
XM_017018212.1:c.615T>C	XP_016873701.1:p.Ile205=
XM_017018213.1:c.600T>C	XP_016873702.1:p.Ile200=
XM_017018214.1:c.597T>C	XP_016873703.1:p.Ile199=
XM_017018215.1:c.591T>C	XP_016873704.1:p.Ile197=
XM_017018216.1:c.651T>C	XP_016873705.1:p.Ile217=
XM_017018217.1:c.630T>C	XP_016873706.1:p.Ile210=
XM_017018218.1:c.618T>C	XP_016873707.1:p.Ile206=
XM_017018219.1:c.579T>C	XP_016873708.1:p.Ile193=
XM_024448669.1:c.630T>C	XP_024304437.1:p.Ile210=
XM_024448670.1:c.612T>C	XP_024304438.1:p.Ile204=
XM_024448671.1:c.609T>C	XP_024304439.1:p.Ile203=
XM_024448672.1:c.591T>C	XP_024304440.1:p.Ile197=
NM_001367842.1:c.630T>C	NP_001354771.1:p.Ile210=
NM_001367843.1:c.630T>C	NP_001354772.1:p.Ile210=
NM_001367844.1:c.612T>C	NP_001354773.1:p.Ile204=
NM_001367845.1:c.612T>C	NP_001354774.1:p.Ile204=
NM_001367846.1:c.669T>C	NP_001354775.1:p.Ile223=
NM_001367847.1:c.645T>C	NP_001354776.1:p.Ile215=
NM_001367848.1:c.633T>C	NP_001354777.1:p.Ile211=
NM_001367849.1:c.624T>C	NP_001354778.1:p.Ile208=
NM_001367850.1:c.579T>C	NP_001354779.1:p.Ile193=
NM_001367851.1:c.432T>C	NP_001354780.1:p.Ile144=
NM_001367852.1:c.432T>C	NP_001354781.1:p.Ile144=
NM_006757.4:c.636T>C MANE Select	NP_006748.1:p.Ile212=
NM_001042780.3:c.612T>C	NP_001036245.1:p.Ile204=
NM_001042781.3:c.630T>C	NP_001036246.1:p.Ile210=
NM_001042782.3:c.612T>C	NP_001036247.1:p.Ile204=
NM_001297646.2:c.612T>C	NP_001284575.1:p.Ile204=
NM_001363561.2:c.645T>C	NP_001350490.1:p.Ile215=