Canonical Allele Identifier: CA1141581495

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359636C= , CM000663.2:g.201359636C=	GRCh38
NC_000001.10:g.201328764C= , CM000663.1:g.201328764C=	GRCh37
NC_000001.9:g.199595387C=	NCBI36
NG_007556.1:g.23042G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.823G=	ENSP00000402238.3:p.Asp275=
ENST00000367318.10:c.808G=	ENSP00000356287.5:p.Asp270=
ENST00000367322.6:c.796G=	ENSP00000356291.2:p.Asp266=
ENST00000412633.3:c.799G=	ENSP00000408731.2:p.Asp267=
ENST00000422165.6:c.829G=	ENSP00000395163.2:p.Asp277=
ENST00000438742.6:c.787G=	ENSP00000414036.2:p.Asp263=
ENST00000651504.1:n.1299G=
ENST00000656932.1:c.838G= MANE Select	ENSP00000499593.1:p.Asp280=
ENST00000658476.1:c.873G=	ENSP00000499741.1:p.Thr291=
ENST00000660295.1:c.808G=	ENSP00000499418.1:p.Asp270=
ENST00000662159.1:c.*197G=	ENSP00000499796.1:n.*197G=
ENST00000663843.1:c.*738G=	ENSP00000499590.1:n.*738G=
ENST00000666449.1:c.*83G=	ENSP00000499667.1:n.*83G=
ENST00000236918.11:c.838G=	ENSP00000236918.8:p.Asp280=
ENST00000360372.8:c.709G=	ENSP00000353535.5:p.Asp237=
ENST00000367315.6:c.817G=	ENSP00000356284.3:p.Asp273=
ENST00000367317.8:c.790G=	ENSP00000356286.5:p.Asp264=
ENST00000367318.9:c.808G=	ENSP00000356287.5:p.Asp270=
ENST00000367320.6:c.709G=	ENSP00000356289.2:p.Asp237=
ENST00000367322.5:c.799G=	ENSP00000356291.1:p.Asp267=
ENST00000421663.6:c.622G=	ENSP00000404134.3:p.Asp208=
ENST00000438742.5:c.790G=	ENSP00000414036.1:p.Asp264=
ENST00000458432.6:c.622G=	ENSP00000387874.3:p.Asp208=
ENST00000460780.5:n.1957G=
ENST00000476888.5:n.255G=
ENST00000491504.5:n.2047G=
ENST00000509001.5:c.808G=	ENSP00000422031.1:p.Asp270=
NM_000364.3:c.829G=	NP_000355.2:p.Asp277=
NM_001001430.2:c.808G=	NP_001001430.1:p.Asp270=
NM_001001431.2:c.799G=	NP_001001431.1:p.Asp267=
NM_001001432.2:c.790G=	NP_001001432.1:p.Asp264=
NM_001276345.1:c.838G=	NP_001263274.1:p.Asp280=
NM_001276346.1:c.709G=	NP_001263275.1:p.Asp237=
NM_001276347.1:c.808G=	NP_001263276.1:p.Asp270=
XM_006711508.2:c.808G=	XP_006711571.1:p.Asp270=
XM_006711509.2:c.805G=	XP_006711572.1:p.Asp269=
XM_011509938.1:c.838G=	XP_011508240.1:p.Asp280=
XM_011509939.1:c.835G=	XP_011508241.1:p.Asp279=
XM_011509940.1:c.835G=	XP_011508242.1:p.Asp279=
XM_011509941.1:c.832G=	XP_011508243.1:p.Asp278=
XM_011509942.1:c.793G=	XP_011508244.1:p.Asp265=
XM_011509943.1:c.793G=	XP_011508245.1:p.Asp265=
XM_011509944.1:c.790G=	XP_011508246.1:p.Asp264=
XM_011509946.1:c.631G=	XP_011508248.1:p.Asp211=
XM_006711508.3:c.808G=	XP_006711571.1:p.Asp270=
XM_006711509.3:c.805G=	XP_006711572.1:p.Asp269=
XM_011509938.2:c.838G=	XP_011508240.1:p.Asp280=
XM_011509940.2:c.835G=	XP_011508242.1:p.Asp279=
XM_011509941.2:c.832G=	XP_011508243.1:p.Asp278=
XM_011509942.2:c.793G=	XP_011508244.1:p.Asp265=
XM_011509943.2:c.793G=	XP_011508245.1:p.Asp265=
XM_011509944.2:c.790G=	XP_011508246.1:p.Asp264=
XM_017002216.2:c.805G=	XP_016857705.1:p.Asp269=
XM_017002217.1:c.799G=	XP_016857706.1:p.Asp267=
XM_024449450.1:c.838G=	XP_024305218.1:p.Asp280=
XM_024449454.1:c.805G=	XP_024305222.1:p.Asp269=
XM_024449455.1:c.805G=	XP_024305223.1:p.Asp269=
NM_000364.4:c.829G=	NP_000355.2:p.Asp277=
NM_001001430.3:c.808G=	NP_001001430.1:p.Asp270=
NM_001001431.3:c.799G=	NP_001001431.1:p.Asp267=
NM_001001432.3:c.790G=	NP_001001432.1:p.Asp264=
NM_001276345.2:c.838G= MANE Select	NP_001263274.1:p.Asp280=
NM_001276346.2:c.709G=	NP_001263275.1:p.Asp237=
NM_001276347.2:c.808G=	NP_001263276.1:p.Asp270=