Canonical Allele Identifier: CA1142337792

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201362019C= , CM000663.2:g.201362019C=	GRCh38
NC_000001.10:g.201331147C= , CM000663.1:g.201331147C=	GRCh37
NC_000001.9:g.199597770C=	NCBI36
NG_007556.1:g.20659G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.598G=	ENSP00000402238.3:p.Glu200=
ENST00000367318.10:c.583G=	ENSP00000356287.5:p.Glu195=
ENST00000367322.6:c.571G=	ENSP00000356291.2:p.Glu191=
ENST00000412633.3:c.574G=	ENSP00000408731.2:p.Glu192=
ENST00000422165.6:c.604G=	ENSP00000395163.2:p.Glu202=
ENST00000438742.6:c.562G=	ENSP00000414036.2:p.Glu188=
ENST00000455702.6:c.598G=	ENSP00000402238.2:p.Glu200=
ENST00000651504.1:n.1074G=
ENST00000656932.1:c.613G= MANE Select	ENSP00000499593.1:p.Glu205=
ENST00000658476.1:c.583G=	ENSP00000499741.1:p.Glu195=
ENST00000660295.1:c.583G=	ENSP00000499418.1:p.Glu195=
ENST00000662159.1:c.163-20G=	ENSP00000499796.1:n.163-20G=
ENST00000663843.1:c.*513G=	ENSP00000499590.1:n.*513G=
ENST00000666449.1:c.583G=	ENSP00000499667.1:p.Glu195=
ENST00000236918.11:c.613G=	ENSP00000236918.8:p.Glu205=
ENST00000360372.8:c.484G=	ENSP00000353535.5:p.Glu162=
ENST00000367315.6:c.592G=	ENSP00000356284.3:p.Glu198=
ENST00000367317.8:c.565G=	ENSP00000356286.5:p.Glu189=
ENST00000367318.9:c.583G=	ENSP00000356287.5:p.Glu195=
ENST00000367320.6:c.484G=	ENSP00000356289.2:p.Glu162=
ENST00000367322.5:c.574G=	ENSP00000356291.1:p.Glu192=
ENST00000421663.6:c.397G=	ENSP00000404134.3:p.Glu133=
ENST00000438742.5:c.565G=	ENSP00000414036.1:p.Glu189=
ENST00000458432.6:c.397G=	ENSP00000387874.3:p.Glu133=
ENST00000460780.5:n.906G=
ENST00000476888.5:n.68G=
ENST00000491504.5:n.1822G=
ENST00000509001.5:c.583G=	ENSP00000422031.1:p.Glu195=
ENST00000515042.5:n.509G=
NM_000364.3:c.604G=	NP_000355.2:p.Glu202=
NM_001001430.2:c.583G=	NP_001001430.1:p.Glu195=
NM_001001431.2:c.574G=	NP_001001431.1:p.Glu192=
NM_001001432.2:c.565G=	NP_001001432.1:p.Glu189=
NM_001276345.1:c.613G=	NP_001263274.1:p.Glu205=
NM_001276346.1:c.484G=	NP_001263275.1:p.Glu162=
NM_001276347.1:c.583G=	NP_001263276.1:p.Glu195=
XM_006711508.2:c.583G=	XP_006711571.1:p.Glu195=
XM_006711509.2:c.580G=	XP_006711572.1:p.Glu194=
XM_011509938.1:c.613G=	XP_011508240.1:p.Glu205=
XM_011509939.1:c.610G=	XP_011508241.1:p.Glu204=
XM_011509940.1:c.610G=	XP_011508242.1:p.Glu204=
XM_011509941.1:c.607G=	XP_011508243.1:p.Glu203=
XM_011509942.1:c.568G=	XP_011508244.1:p.Glu190=
XM_011509943.1:c.568G=	XP_011508245.1:p.Glu190=
XM_011509944.1:c.565G=	XP_011508246.1:p.Glu189=
XM_011509946.1:c.406G=	XP_011508248.1:p.Glu136=
XM_006711508.3:c.583G=	XP_006711571.1:p.Glu195=
XM_006711509.3:c.580G=	XP_006711572.1:p.Glu194=
XM_011509938.2:c.613G=	XP_011508240.1:p.Glu205=
XM_011509940.2:c.610G=	XP_011508242.1:p.Glu204=
XM_011509941.2:c.607G=	XP_011508243.1:p.Glu203=
XM_011509942.2:c.568G=	XP_011508244.1:p.Glu190=
XM_011509943.2:c.568G=	XP_011508245.1:p.Glu190=
XM_011509944.2:c.565G=	XP_011508246.1:p.Glu189=
XM_017002216.2:c.580G=	XP_016857705.1:p.Glu194=
XM_017002217.1:c.574G=	XP_016857706.1:p.Glu192=
XM_024449450.1:c.613G=	XP_024305218.1:p.Glu205=
XM_024449454.1:c.580G=	XP_024305222.1:p.Glu194=
XM_024449455.1:c.580G=	XP_024305223.1:p.Glu194=
NM_000364.4:c.604G=	NP_000355.2:p.Glu202=
NM_001001430.3:c.583G=	NP_001001430.1:p.Glu195=
NM_001001431.3:c.574G=	NP_001001431.1:p.Glu192=
NM_001001432.3:c.565G=	NP_001001432.1:p.Glu189=
NM_001276345.2:c.613G= MANE Select	NP_001263274.1:p.Glu205=
NM_001276346.2:c.484G=	NP_001263275.1:p.Glu162=
NM_001276347.2:c.583G=	NP_001263276.1:p.Glu195=