Canonical Allele Identifier: CA077561

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359244C>T , CM000663.2:g.201359244C>T	GRCh38
NC_000001.10:g.201328372C>T , CM000663.1:g.201328372C>T	GRCh37
NC_000001.9:g.199594995C>T	NCBI36
NG_007556.1:g.23434G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.848G>A	ENSP00000402238.3:p.Arg283His
ENST00000367318.10:c.833G>A	ENSP00000356287.5:p.Arg278His
ENST00000367322.6:c.821G>A	ENSP00000356291.2:p.Arg274His
ENST00000412633.3:c.824G>A	ENSP00000408731.2:p.Arg275His
ENST00000422165.6:c.854G>A	ENSP00000395163.2:p.Arg285His
ENST00000438742.6:c.812G>A	ENSP00000414036.2:p.Arg271His
ENST00000651504.1:n.1324G>A
ENST00000656932.1:c.863G>A MANE Select	ENSP00000499593.1:p.Arg288His
ENST00000658476.1:c.898G>A	ENSP00000499741.1:p.Ala300Thr
ENST00000660295.1:c.833G>A	ENSP00000499418.1:p.Arg278His
ENST00000662159.1:c.*222G>A	ENSP00000499796.1:n.*222G>A
ENST00000663843.1:c.*763G>A	ENSP00000499590.1:n.*763G>A
ENST00000666449.1:c.*108G>A	ENSP00000499667.1:n.*108G>A
ENST00000236918.11:c.863G>A	ENSP00000236918.8:p.Arg288His
ENST00000360372.8:c.734G>A	ENSP00000353535.5:p.Arg245His
ENST00000367315.6:c.842G>A	ENSP00000356284.3:p.Arg281His
ENST00000367317.8:c.815G>A	ENSP00000356286.5:p.Arg272His
ENST00000367318.9:c.833G>A	ENSP00000356287.5:p.Arg278His
ENST00000367320.6:c.734G>A	ENSP00000356289.2:p.Arg245His
ENST00000367322.5:c.824G>A	ENSP00000356291.1:p.Arg275His
ENST00000421663.6:c.647G>A	ENSP00000404134.3:p.Arg216His
ENST00000458432.6:c.647G>A	ENSP00000387874.3:p.Arg216His
ENST00000460780.5:n.1982G>A
ENST00000476888.5:n.280G>A
ENST00000491504.5:n.2072G>A
ENST00000509001.5:c.833G>A	ENSP00000422031.1:p.Arg278His
NM_000364.3:c.854G>A	NP_000355.2:p.Arg285His
NM_001001430.2:c.833G>A	NP_001001430.1:p.Arg278His
NM_001001431.2:c.824G>A	NP_001001431.1:p.Arg275His
NM_001001432.2:c.815G>A	NP_001001432.1:p.Arg272His
NM_001276345.1:c.863G>A	NP_001263274.1:p.Arg288His
NM_001276346.1:c.734G>A	NP_001263275.1:p.Arg245His
NM_001276347.1:c.833G>A	NP_001263276.1:p.Arg278His
XM_006711508.2:c.833G>A	XP_006711571.1:p.Arg278His
XM_006711509.2:c.830G>A	XP_006711572.1:p.Arg277His
XM_011509938.1:c.863G>A	XP_011508240.1:p.Arg288His
XM_011509939.1:c.860G>A	XP_011508241.1:p.Arg287His
XM_011509940.1:c.860G>A	XP_011508242.1:p.Arg287His
XM_011509941.1:c.857G>A	XP_011508243.1:p.Arg286His
XM_011509942.1:c.818G>A	XP_011508244.1:p.Arg273His
XM_011509943.1:c.818G>A	XP_011508245.1:p.Arg273His
XM_011509944.1:c.815G>A	XP_011508246.1:p.Arg272His
XM_011509946.1:c.656G>A	XP_011508248.1:p.Arg219His
XM_006711508.3:c.833G>A	XP_006711571.1:p.Arg278His
XM_006711509.3:c.830G>A	XP_006711572.1:p.Arg277His
XM_011509938.2:c.863G>A	XP_011508240.1:p.Arg288His
XM_011509940.2:c.860G>A	XP_011508242.1:p.Arg287His
XM_011509941.2:c.857G>A	XP_011508243.1:p.Arg286His
XM_011509942.2:c.818G>A	XP_011508244.1:p.Arg273His
XM_011509943.2:c.818G>A	XP_011508245.1:p.Arg273His
XM_011509944.2:c.815G>A	XP_011508246.1:p.Arg272His
XM_017002216.2:c.830G>A	XP_016857705.1:p.Arg277His
XM_017002217.1:c.824G>A	XP_016857706.1:p.Arg275His
XM_024449450.1:c.863G>A	XP_024305218.1:p.Arg288His
XM_024449454.1:c.830G>A	XP_024305222.1:p.Arg277His
XM_024449455.1:c.830G>A	XP_024305223.1:p.Arg277His
NM_000364.4:c.854G>A	NP_000355.2:p.Arg285His
NM_001001430.3:c.833G>A	NP_001001430.1:p.Arg278His
NM_001001431.3:c.824G>A	NP_001001431.1:p.Arg275His
NM_001001432.3:c.815G>A	NP_001001432.1:p.Arg272His
NM_001276345.2:c.863G>A MANE Select	NP_001263274.1:p.Arg288His
NM_001276346.2:c.734G>A	NP_001263275.1:p.Arg245His
NM_001276347.2:c.833G>A	NP_001263276.1:p.Arg278His