Canonical Allele Identifier: CA1141581494

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359245G= , CM000663.2:g.201359245G=	GRCh38
NC_000001.10:g.201328373G= , CM000663.1:g.201328373G=	GRCh37
NC_000001.9:g.199594996G=	NCBI36
NG_007556.1:g.23433C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.847C=	ENSP00000402238.3:p.Arg283=
ENST00000367318.10:c.832C=	ENSP00000356287.5:p.Arg278=
ENST00000367322.6:c.820C=	ENSP00000356291.2:p.Arg274=
ENST00000412633.3:c.823C=	ENSP00000408731.2:p.Arg275=
ENST00000422165.6:c.853C=	ENSP00000395163.2:p.Arg285=
ENST00000438742.6:c.811C=	ENSP00000414036.2:p.Arg271=
ENST00000651504.1:n.1323C=
ENST00000656932.1:c.862C= MANE Select	ENSP00000499593.1:p.Arg288=
ENST00000658476.1:c.897C=	ENSP00000499741.1:p.Pro299=
ENST00000660295.1:c.832C=	ENSP00000499418.1:p.Arg278=
ENST00000662159.1:c.*221C=	ENSP00000499796.1:n.*221C=
ENST00000663843.1:c.*762C=	ENSP00000499590.1:n.*762C=
ENST00000666449.1:c.*107C=	ENSP00000499667.1:n.*107C=
ENST00000236918.11:c.862C=	ENSP00000236918.8:p.Arg288=
ENST00000360372.8:c.733C=	ENSP00000353535.5:p.Arg245=
ENST00000367315.6:c.841C=	ENSP00000356284.3:p.Arg281=
ENST00000367317.8:c.814C=	ENSP00000356286.5:p.Arg272=
ENST00000367318.9:c.832C=	ENSP00000356287.5:p.Arg278=
ENST00000367320.6:c.733C=	ENSP00000356289.2:p.Arg245=
ENST00000367322.5:c.823C=	ENSP00000356291.1:p.Arg275=
ENST00000421663.6:c.646C=	ENSP00000404134.3:p.Arg216=
ENST00000438742.5:c.814C=
ENST00000458432.6:c.646C=	ENSP00000387874.3:p.Arg216=
ENST00000460780.5:n.1981C=
ENST00000476888.5:n.279C=
ENST00000491504.5:n.2071C=
ENST00000509001.5:c.832C=	ENSP00000422031.1:p.Arg278=
NM_000364.3:c.853C=	NP_000355.2:p.Arg285=
NM_001001430.2:c.832C=	NP_001001430.1:p.Arg278=
NM_001001431.2:c.823C=	NP_001001431.1:p.Arg275=
NM_001001432.2:c.814C=	NP_001001432.1:p.Arg272=
NM_001276345.1:c.862C=	NP_001263274.1:p.Arg288=
NM_001276346.1:c.733C=	NP_001263275.1:p.Arg245=
NM_001276347.1:c.832C=	NP_001263276.1:p.Arg278=
XM_006711508.2:c.832C=	XP_006711571.1:p.Arg278=
XM_006711509.2:c.829C=	XP_006711572.1:p.Arg277=
XM_011509938.1:c.862C=	XP_011508240.1:p.Arg288=
XM_011509939.1:c.859C=	XP_011508241.1:p.Arg287=
XM_011509940.1:c.859C=	XP_011508242.1:p.Arg287=
XM_011509941.1:c.856C=	XP_011508243.1:p.Arg286=
XM_011509942.1:c.817C=	XP_011508244.1:p.Arg273=
XM_011509943.1:c.817C=	XP_011508245.1:p.Arg273=
XM_011509944.1:c.814C=	XP_011508246.1:p.Arg272=
XM_011509946.1:c.655C=	XP_011508248.1:p.Arg219=
XM_006711508.3:c.832C=	XP_006711571.1:p.Arg278=
XM_006711509.3:c.829C=	XP_006711572.1:p.Arg277=
XM_011509938.2:c.862C=	XP_011508240.1:p.Arg288=
XM_011509940.2:c.859C=	XP_011508242.1:p.Arg287=
XM_011509941.2:c.856C=	XP_011508243.1:p.Arg286=
XM_011509942.2:c.817C=	XP_011508244.1:p.Arg273=
XM_011509943.2:c.817C=	XP_011508245.1:p.Arg273=
XM_011509944.2:c.814C=	XP_011508246.1:p.Arg272=
XM_017002216.2:c.829C=	XP_016857705.1:p.Arg277=
XM_017002217.1:c.823C=	XP_016857706.1:p.Arg275=
XM_024449450.1:c.862C=	XP_024305218.1:p.Arg288=
XM_024449454.1:c.829C=	XP_024305222.1:p.Arg277=
XM_024449455.1:c.829C=	XP_024305223.1:p.Arg277=
NM_000364.4:c.853C=	NP_000355.2:p.Arg285=
NM_001001430.3:c.832C=	NP_001001430.1:p.Arg278=
NM_001001431.3:c.823C=	NP_001001431.1:p.Arg275=
NM_001001432.3:c.814C=	NP_001001432.1:p.Arg272=
NM_001276345.2:c.862C= MANE Select	NP_001263274.1:p.Arg288=
NM_001276346.2:c.733C=	NP_001263275.1:p.Arg245=
NM_001276347.2:c.832C=	NP_001263276.1:p.Arg278=