Canonical Allele Identifier: CA1140026365

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359639T= , CM000663.2:g.201359639T=	GRCh38
NC_000001.10:g.201328767T= , CM000663.1:g.201328767T=	GRCh37
NC_000001.9:g.199595390T=	NCBI36
NG_007556.1:g.23039A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.820A=	ENSP00000402238.3:p.Asn274=
ENST00000367318.10:c.805A=	ENSP00000356287.5:p.Asn269=
ENST00000367322.6:c.793A=	ENSP00000356291.2:p.Asn265=
ENST00000412633.3:c.796A=	ENSP00000408731.2:p.Asn266=
ENST00000422165.6:c.826A=	ENSP00000395163.2:p.Asn276=
ENST00000438742.6:c.784A=	ENSP00000414036.2:p.Asn262=
ENST00000651504.1:n.1296A=
ENST00000656932.1:c.835A= MANE Select	ENSP00000499593.1:p.Asn279=
ENST00000658476.1:c.870A=	ENSP00000499741.1:p.Ser290=
ENST00000660295.1:c.805A=	ENSP00000499418.1:p.Asn269=
ENST00000662159.1:c.*194A=	ENSP00000499796.1:n.*194A=
ENST00000663843.1:c.*735A=	ENSP00000499590.1:n.*735A=
ENST00000666449.1:c.*80A=	ENSP00000499667.1:n.*80A=
ENST00000236918.11:c.835A=	ENSP00000236918.8:p.Asn279=
ENST00000360372.8:c.706A=	ENSP00000353535.5:p.Asn236=
ENST00000367315.6:c.814A=	ENSP00000356284.3:p.Asn272=
ENST00000367317.8:c.787A=	ENSP00000356286.5:p.Asn263=
ENST00000367318.9:c.805A=	ENSP00000356287.5:p.Asn269=
ENST00000367320.6:c.706A=	ENSP00000356289.2:p.Asn236=
ENST00000367322.5:c.796A=	ENSP00000356291.1:p.Asn266=
ENST00000421663.6:c.619A=	ENSP00000404134.3:p.Asn207=
ENST00000438742.5:c.787A=	ENSP00000414036.1:p.Asn263=
ENST00000458432.6:c.619A=	ENSP00000387874.3:p.Asn207=
ENST00000460780.5:n.1954A=
ENST00000476888.5:n.252A=
ENST00000491504.5:n.2044A=
ENST00000509001.5:c.805A=	ENSP00000422031.1:p.Asn269=
NM_000364.3:c.826A=	NP_000355.2:p.Asn276=
NM_001001430.2:c.805A=	NP_001001430.1:p.Asn269=
NM_001001431.2:c.796A=	NP_001001431.1:p.Asn266=
NM_001001432.2:c.787A=	NP_001001432.1:p.Asn263=
NM_001276345.1:c.835A=	NP_001263274.1:p.Asn279=
NM_001276346.1:c.706A=	NP_001263275.1:p.Asn236=
NM_001276347.1:c.805A=	NP_001263276.1:p.Asn269=
XM_006711508.2:c.805A=	XP_006711571.1:p.Asn269=
XM_006711509.2:c.802A=	XP_006711572.1:p.Asn268=
XM_011509938.1:c.835A=	XP_011508240.1:p.Asn279=
XM_011509939.1:c.832A=	XP_011508241.1:p.Asn278=
XM_011509940.1:c.832A=	XP_011508242.1:p.Asn278=
XM_011509941.1:c.829A=	XP_011508243.1:p.Asn277=
XM_011509942.1:c.790A=	XP_011508244.1:p.Asn264=
XM_011509943.1:c.790A=	XP_011508245.1:p.Asn264=
XM_011509944.1:c.787A=	XP_011508246.1:p.Asn263=
XM_011509946.1:c.628A=	XP_011508248.1:p.Asn210=
XM_006711508.3:c.805A=	XP_006711571.1:p.Asn269=
XM_006711509.3:c.802A=	XP_006711572.1:p.Asn268=
XM_011509938.2:c.835A=	XP_011508240.1:p.Asn279=
XM_011509940.2:c.832A=	XP_011508242.1:p.Asn278=
XM_011509941.2:c.829A=	XP_011508243.1:p.Asn277=
XM_011509942.2:c.790A=	XP_011508244.1:p.Asn264=
XM_011509943.2:c.790A=	XP_011508245.1:p.Asn264=
XM_011509944.2:c.787A=	XP_011508246.1:p.Asn263=
XM_017002216.2:c.802A=	XP_016857705.1:p.Asn268=
XM_017002217.1:c.796A=	XP_016857706.1:p.Asn266=
XM_024449450.1:c.835A=	XP_024305218.1:p.Asn279=
XM_024449454.1:c.802A=	XP_024305222.1:p.Asn268=
XM_024449455.1:c.802A=	XP_024305223.1:p.Asn268=
NM_000364.4:c.826A=	NP_000355.2:p.Asn276=
NM_001001430.3:c.805A=	NP_001001430.1:p.Asn269=
NM_001001431.3:c.796A=	NP_001001431.1:p.Asn266=
NM_001001432.3:c.787A=	NP_001001432.1:p.Asn263=
NM_001276345.2:c.835A= MANE Select	NP_001263274.1:p.Asn279=
NM_001276346.2:c.706A=	NP_001263275.1:p.Asn236=
NM_001276347.2:c.805A=	NP_001263276.1:p.Asn269=