Canonical Allele Identifier: CA089792

Gene: TNNT2

Linked Data

• MyVariant Identifiers: chr1:g.201334349C>G (hg19) ; chr1:g.201365221C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201365221C>G , CM000663.2:g.201365221C>G	GRCh38
NC_000001.10:g.201334349C>G , CM000663.1:g.201334349C>G	GRCh37
NC_000001.9:g.199600972C>G	NCBI36
NG_007556.1:g.17457G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.366G>C	ENSP00000402238.3:p.Glu122Asp
ENST00000367318.10:c.351G>C	ENSP00000356287.5:p.Glu117Asp
ENST00000367322.6:c.348G>C	ENSP00000356291.2:p.Glu116Asp
ENST00000412633.3:c.351G>C	ENSP00000408731.2:p.Glu117Asp
ENST00000422165.6:c.381G>C	ENSP00000395163.2:p.Glu127Asp
ENST00000438742.6:c.333G>C	ENSP00000414036.2:p.Glu111Asp
ENST00000455702.6:c.366G>C	ENSP00000402238.2:p.Glu122Asp
ENST00000651504.1:n.845G>C
ENST00000656932.1:c.381G>C MANE Select	ENSP00000499593.1:p.Glu127Asp
ENST00000658476.1:c.351G>C	ENSP00000499741.1:p.Glu117Asp
ENST00000660295.1:c.351G>C	ENSP00000499418.1:p.Glu117Asp
ENST00000662159.1:c.162+2557G>C	ENSP00000499796.1:n.162+2557G>C
ENST00000663843.1:c.*281G>C	ENSP00000499590.1:n.*281G>C
ENST00000666449.1:c.351G>C	ENSP00000499667.1:p.Glu117Asp
ENST00000236918.11:c.381G>C	ENSP00000236918.8:p.Glu127Asp
ENST00000360372.8:c.291+389G>C	ENSP00000353535.5:n.291+389G>C
ENST00000367315.6:c.357G>C	ENSP00000356284.3:p.Glu119Asp
ENST00000367317.8:c.336G>C	ENSP00000356286.5:p.Glu112Asp
ENST00000367318.9:c.351G>C	ENSP00000356287.5:p.Glu117Asp
ENST00000367320.6:c.291+389G>C	ENSP00000356289.2:n.291+389G>C
ENST00000367322.5:c.351G>C	ENSP00000356291.1:p.Glu117Asp
ENST00000421663.6:c.174G>C	ENSP00000404134.3:p.Glu58Asp
ENST00000438742.5:c.336G>C	ENSP00000414036.1:p.Glu112Asp
ENST00000455702.5:c.381G>C	ENSP00000402238.1:p.Glu127Asp
ENST00000458432.6:c.174G>C	ENSP00000387874.3:p.Glu58Asp
ENST00000466570.5:n.607G>C
ENST00000491504.5:n.1590G>C
ENST00000503459.1:n.220G>C
ENST00000509001.5:c.351G>C	ENSP00000422031.1:p.Glu117Asp
ENST00000515042.5:n.277G>C
NM_000364.3:c.381G>C	NP_000355.2:p.Glu127Asp
NM_001001430.2:c.351G>C	NP_001001430.1:p.Glu117Asp
NM_001001431.2:c.351G>C	NP_001001431.1:p.Glu117Asp
NM_001001432.2:c.336G>C	NP_001001432.1:p.Glu112Asp
NM_001276345.1:c.381G>C	NP_001263274.1:p.Glu127Asp
NM_001276346.1:c.291+389G>C	NP_001263275.1:n.291+389G>C
NM_001276347.1:c.351G>C	NP_001263276.1:p.Glu117Asp
XM_006711508.2:c.351G>C	XP_006711571.1:p.Glu117Asp
XM_006711509.2:c.348G>C	XP_006711572.1:p.Glu116Asp
XM_011509938.1:c.381G>C	XP_011508240.1:p.Glu127Asp
XM_011509939.1:c.378G>C	XP_011508241.1:p.Glu126Asp
XM_011509940.1:c.381G>C	XP_011508242.1:p.Glu127Asp
XM_011509941.1:c.378G>C	XP_011508243.1:p.Glu126Asp
XM_011509942.1:c.336G>C	XP_011508244.1:p.Glu112Asp
XM_011509943.1:c.336G>C	XP_011508245.1:p.Glu112Asp
XM_011509944.1:c.333G>C	XP_011508246.1:p.Glu111Asp
XM_011509945.1:c.381G>C	XP_011508247.1:p.Glu127Asp
XM_011509946.1:c.174G>C	XP_011508248.1:p.Glu58Asp
XM_006711508.3:c.351G>C	XP_006711571.1:p.Glu117Asp
XM_006711509.3:c.348G>C	XP_006711572.1:p.Glu116Asp
XM_011509938.2:c.381G>C	XP_011508240.1:p.Glu127Asp
XM_011509940.2:c.381G>C	XP_011508242.1:p.Glu127Asp
XM_011509941.2:c.378G>C	XP_011508243.1:p.Glu126Asp
XM_011509942.2:c.336G>C	XP_011508244.1:p.Glu112Asp
XM_011509943.2:c.336G>C	XP_011508245.1:p.Glu112Asp
XM_011509944.2:c.333G>C	XP_011508246.1:p.Glu111Asp
XM_017002216.2:c.351G>C	XP_016857705.1:p.Glu117Asp
XM_017002217.1:c.351G>C	XP_016857706.1:p.Glu117Asp
XM_024449450.1:c.381G>C	XP_024305218.1:p.Glu127Asp
XM_024449454.1:c.348G>C	XP_024305222.1:p.Glu116Asp
XM_024449455.1:c.351G>C	XP_024305223.1:p.Glu117Asp
NM_000364.4:c.381G>C	NP_000355.2:p.Glu127Asp
NM_001001430.3:c.351G>C	NP_001001430.1:p.Glu117Asp
NM_001001431.3:c.351G>C	NP_001001431.1:p.Glu117Asp
NM_001001432.3:c.336G>C	NP_001001432.1:p.Glu112Asp
NM_001276345.2:c.381G>C MANE Select	NP_001263274.1:p.Glu127Asp
NM_001276346.2:c.291+389G>C	NP_001263275.1:n.291+389G>C
NM_001276347.2:c.351G>C	NP_001263276.1:p.Glu117Asp