Canonical Allele Identifier: CA208350

Gene: TNNT3

Linked Data

• ClinVar Variation Id: 31874
• ClinVar RCV Id: RCV000024570 ; RCV000194279 ; RCV000787280
• dbSNP Id: rs199474721
• MyVariant Identifiers: chr11:g.1954966C>T (hg19) ; chr11:g.1933736C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1933736C>T , CM000673.2:g.1933736C>T	GRCh38
NC_000011.9:g.1954966C>T , CM000673.1:g.1954966C>T	GRCh37
NC_000011.8:g.1911542C>T	NCBI36
NG_013085.1:g.19168C>T
NG_013085.2:g.19168C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706488.1:c.181C>T	ENSP00000516410.1:p.Arg61Cys
ENST00000278317.11:c.187C>T MANE Select	ENSP00000278317.6:p.Arg63Cys
ENST00000381558.6:c.163C>T	ENSP00000370970.1:p.Arg55Cys
ENST00000639560.1:n.297C>T
ENST00000641119.1:c.181C>T	ENSP00000492914.1:p.Arg61Cys
ENST00000641225.1:c.-18C>T	ENSP00000493372.1:n.-18C>T
ENST00000641787.1:c.163C>T	ENSP00000493331.1:p.Arg55Cys
ENST00000278317.10:c.187C>T	ENSP00000278317.6:p.Arg63Cys
ENST00000344578.8:c.148C>T	ENSP00000344870.4:p.Arg50Cys
ENST00000381557.6:c.145C>T	ENSP00000370969.2:p.Arg49Cys
ENST00000381558.5:c.163C>T	ENSP00000370970.1:p.Arg55Cys
ENST00000381563.8:c.196C>T	ENSP00000370975.4:p.Arg66Cys
ENST00000381579.7:c.163C>T	ENSP00000370991.3:p.Arg55Cys
ENST00000381589.7:c.181C>T	ENSP00000371001.3:p.Arg61Cys
ENST00000397301.5:c.220C>T	ENSP00000380468.1:p.Arg74Cys
ENST00000397304.6:c.130C>T	ENSP00000380471.2:p.Arg44Cys
ENST00000446240.1:c.130C>T	ENSP00000413203.1:p.Arg44Cys
ENST00000453458.5:c.130C>T	ENSP00000415614.1:p.Arg44Cys
ENST00000492075.5:n.404C>T
NM_001042780.2:c.163C>T	NP_001036245.1:p.Arg55Cys
NM_001042781.2:c.181C>T	NP_001036246.1:p.Arg61Cys
NM_001042782.2:c.163C>T	NP_001036247.1:p.Arg55Cys
NM_001297646.1:c.163C>T	NP_001284575.1:p.Arg55Cys
NM_006757.3:c.187C>T	NP_006748.1:p.Arg63Cys
XM_006718288.2:c.235C>T	XP_006718351.1:p.Arg79Cys
XM_006718290.2:c.220C>T	XP_006718353.1:p.Arg74Cys
XM_006718291.2:c.208C>T	XP_006718354.1:p.Arg70Cys
XM_006718292.2:c.199C>T	XP_006718355.1:p.Arg67Cys
XM_006718293.1:c.196C>T	XP_006718356.1:p.Arg66Cys
XM_006718294.2:c.196C>T	XP_006718357.1:p.Arg66Cys
XM_006718295.2:c.193C>T	XP_006718358.1:p.Arg65Cys
XM_006718296.2:c.184C>T	XP_006718359.1:p.Arg62Cys
XM_006718297.2:c.175C>T	XP_006718360.1:p.Arg59Cys
XM_006718298.2:c.169C>T	XP_006718361.1:p.Arg57Cys
XM_006718299.1:c.160C>T	XP_006718362.1:p.Arg54Cys
XM_006718300.2:c.148C>T	XP_006718363.1:p.Arg50Cys
XM_006718301.2:c.148C>T	XP_006718364.1:p.Arg50Cys
XM_006718302.2:c.130C>T	XP_006718365.1:p.Arg44Cys
XM_011520342.1:c.220C>T	XP_011518644.1:p.Arg74Cys
XM_011520343.1:c.220C>T	XP_011518645.1:p.Arg74Cys
NM_001363561.1:c.196C>T	NP_001350490.1:p.Arg66Cys
XM_006718288.3:c.235C>T	XP_006718351.1:p.Arg79Cys
XM_006718290.3:c.220C>T	XP_006718353.1:p.Arg74Cys
XM_006718294.3:c.196C>T	XP_006718357.1:p.Arg66Cys
XM_006718296.3:c.184C>T	XP_006718359.1:p.Arg62Cys
XM_006718299.2:c.160C>T	XP_006718362.1:p.Arg54Cys
XM_006718300.3:c.148C>T	XP_006718363.1:p.Arg50Cys
XM_006718302.3:c.130C>T	XP_006718365.1:p.Arg44Cys
XM_011520343.2:c.220C>T	XP_011518645.1:p.Arg74Cys
XM_017018205.1:c.181C>T	XP_016873694.1:p.Arg61Cys
XM_017018206.1:c.220C>T	XP_016873695.1:p.Arg74Cys
XM_017018207.1:c.208C>T	XP_016873696.1:p.Arg70Cys
XM_017018208.1:c.199C>T	XP_016873697.1:p.Arg67Cys
XM_017018209.1:c.184C>T	XP_016873698.1:p.Arg62Cys
XM_017018210.1:c.175C>T	XP_016873699.1:p.Arg59Cys
XM_017018211.1:c.169C>T	XP_016873700.1:p.Arg57Cys
XM_017018212.1:c.166C>T	XP_016873701.1:p.Arg56Cys
XM_017018213.1:c.151C>T	XP_016873702.1:p.Arg51Cys
XM_017018214.1:c.148C>T	XP_016873703.1:p.Arg50Cys
XM_017018215.1:c.142C>T	XP_016873704.1:p.Arg48Cys
XM_017018216.1:c.202C>T	XP_016873705.1:p.Arg68Cys
XM_017018217.1:c.181C>T	XP_016873706.1:p.Arg61Cys
XM_017018218.1:c.169C>T	XP_016873707.1:p.Arg57Cys
XM_017018219.1:c.130C>T	XP_016873708.1:p.Arg44Cys
XM_024448669.1:c.181C>T	XP_024304437.1:p.Arg61Cys
XM_024448670.1:c.163C>T	XP_024304438.1:p.Arg55Cys
XM_024448671.1:c.160C>T	XP_024304439.1:p.Arg54Cys
XM_024448672.1:c.142C>T	XP_024304440.1:p.Arg48Cys
NM_001367842.1:c.181C>T	NP_001354771.1:p.Arg61Cys
NM_001367843.1:c.181C>T	NP_001354772.1:p.Arg61Cys
NM_001367844.1:c.163C>T	NP_001354773.1:p.Arg55Cys
NM_001367845.1:c.163C>T	NP_001354774.1:p.Arg55Cys
NM_001367846.1:c.220C>T	NP_001354775.1:p.Arg74Cys
NM_001367847.1:c.196C>T	NP_001354776.1:p.Arg66Cys
NM_001367848.1:c.184C>T	NP_001354777.1:p.Arg62Cys
NM_001367849.1:c.175C>T	NP_001354778.1:p.Arg59Cys
NM_001367850.1:c.130C>T	NP_001354779.1:p.Arg44Cys
NM_001367851.1:c.-18C>T	NP_001354780.1:n.-18C>T
NM_001367852.1:c.-18C>T	NP_001354781.1:n.-18C>T
NM_006757.4:c.187C>T MANE Select	NP_006748.1:p.Arg63Cys
NM_001042780.3:c.163C>T	NP_001036245.1:p.Arg55Cys
NM_001042781.3:c.181C>T	NP_001036246.1:p.Arg61Cys
NM_001042782.3:c.163C>T	NP_001036247.1:p.Arg55Cys
NM_001297646.2:c.163C>T	NP_001284575.1:p.Arg55Cys
NM_001363561.2:c.196C>T	NP_001350490.1:p.Arg66Cys