Canonical Allele Identifier: CA1219715233

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201373157G= , CM000663.2:g.201373157G=	GRCh38
NC_000001.10:g.201342285G= , CM000663.1:g.201342285G=	GRCh37
NC_000001.9:g.199608908G=	NCBI36
NG_007556.1:g.9521C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.41+57C=	ENSP00000402238.3:n.41+57C=
ENST00000367318.10:c.41+57C=	ENSP00000356287.5:n.41+57C=
ENST00000367322.6:c.41+57C=	ENSP00000356291.2:n.41+57C=
ENST00000412633.3:c.41+57C=	ENSP00000408731.2:n.41+57C=
ENST00000422165.6:c.41+57C=	ENSP00000395163.2:n.41+57C=
ENST00000438742.6:c.41+57C=	ENSP00000414036.2:n.41+57C=
ENST00000455702.6:c.41+57C=	ENSP00000402238.2:n.41+57C=
ENST00000656932.1:c.41+57C= MANE Select	ENSP00000499593.1:n.41+57C=
ENST00000658476.1:c.41+57C=	ENSP00000499741.1:n.41+57C=
ENST00000660295.1:c.41+57C=	ENSP00000499418.1:n.41+57C=
ENST00000662159.1:c.41+57C=	ENSP00000499796.1:n.41+57C=
ENST00000663843.1:c.41+57C=	ENSP00000499590.1:n.41+57C=
ENST00000666449.1:c.41+57C=	ENSP00000499667.1:n.41+57C=
ENST00000236918.11:c.41+57C=	ENSP00000236918.8:n.41+57C=
ENST00000360372.8:c.41+57C=	ENSP00000353535.5:n.41+57C=
ENST00000367315.6:c.54+40C=	ENSP00000356284.3:n.54+40C=
ENST00000367317.8:c.41+57C=	ENSP00000356286.5:n.41+57C=
ENST00000367318.9:c.41+57C=	ENSP00000356287.5:n.41+57C=
ENST00000367320.6:c.41+57C=	ENSP00000356289.2:n.41+57C=
ENST00000367322.5:c.41+57C=	ENSP00000356291.1:n.41+57C=
ENST00000412633.2:c.41+57C=	ENSP00000408731.1:n.41+57C=
ENST00000421663.6:c.-111+52C=	ENSP00000404134.3:n.-111+52C=
ENST00000422165.5:c.41+57C=	ENSP00000395163.1:n.41+57C=
ENST00000438742.5:c.41+57C=	ENSP00000414036.1:n.41+57C=
ENST00000455702.5:c.41+57C=	ENSP00000402238.1:n.41+57C=
ENST00000458432.6:c.-160+49C=	ENSP00000387874.3:n.-160+49C=
ENST00000466570.5:n.159C=
ENST00000472177.2:n.113+57C=
ENST00000475686.5:n.109C=
ENST00000491504.5:n.113+57C=
ENST00000494095.5:n.2155+57C=
ENST00000509001.5:c.41+57C=	ENSP00000422031.1:n.41+57C=
NM_000364.3:c.41+57C=	NP_000355.2:n.41+57C=
NM_001001430.2:c.41+57C=	NP_001001430.1:n.41+57C=
NM_001001431.2:c.41+57C=	NP_001001431.1:n.41+57C=
NM_001001432.2:c.41+57C=	NP_001001432.1:n.41+57C=
NM_001276345.1:c.41+57C=	NP_001263274.1:n.41+57C=
NM_001276346.1:c.41+57C=	NP_001263275.1:n.41+57C=
NM_001276347.1:c.41+57C=	NP_001263276.1:n.41+57C=
XM_006711508.2:c.41+57C=	XP_006711571.1:n.41+57C=
XM_006711509.2:c.41+57C=	XP_006711572.1:n.41+57C=
XM_011509938.1:c.41+57C=	XP_011508240.1:n.41+57C=
XM_011509939.1:c.41+57C=	XP_011508241.1:n.41+57C=
XM_011509940.1:c.41+57C=	XP_011508242.1:n.41+57C=
XM_011509941.1:c.41+57C=	XP_011508243.1:n.41+57C=
XM_011509942.1:c.41+57C=	XP_011508244.1:n.41+57C=
XM_011509943.1:c.41+57C=	XP_011508245.1:n.41+57C=
XM_011509944.1:c.41+57C=	XP_011508246.1:n.41+57C=
XM_011509945.1:c.41+57C=	XP_011508247.1:n.41+57C=
XM_011509946.1:c.-175C=	XP_011508248.1:n.-175C=
XM_006711508.3:c.41+57C=	XP_006711571.1:n.41+57C=
XM_006711509.3:c.41+57C=	XP_006711572.1:n.41+57C=
XM_011509938.2:c.41+57C=	XP_011508240.1:n.41+57C=
XM_011509940.2:c.41+57C=	XP_011508242.1:n.41+57C=
XM_011509941.2:c.41+57C=	XP_011508243.1:n.41+57C=
XM_011509942.2:c.41+57C=	XP_011508244.1:n.41+57C=
XM_011509943.2:c.41+57C=	XP_011508245.1:n.41+57C=
XM_011509944.2:c.41+57C=	XP_011508246.1:n.41+57C=
XM_017002216.2:c.41+57C=	XP_016857705.1:n.41+57C=
XM_017002217.1:c.41+57C=	XP_016857706.1:n.41+57C=
XM_024449450.1:c.41+57C=	XP_024305218.1:n.41+57C=
XM_024449454.1:c.41+57C=	XP_024305222.1:n.41+57C=
XM_024449455.1:c.41+57C=	XP_024305223.1:n.41+57C=
NM_000364.4:c.41+57C=	NP_000355.2:n.41+57C=
NM_001001430.3:c.41+57C=	NP_001001430.1:n.41+57C=
NM_001001431.3:c.41+57C=	NP_001001431.1:n.41+57C=
NM_001001432.3:c.41+57C=	NP_001001432.1:n.41+57C=
NM_001276345.2:c.41+57C= MANE Select	NP_001263274.1:n.41+57C=
NM_001276346.2:c.41+57C=	NP_001263275.1:n.41+57C=
NM_001276347.2:c.41+57C=	NP_001263276.1:n.41+57C=