Canonical Allele Identifier: CA1219709403

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359228G= , CM000663.2:g.201359228G=	GRCh38
NC_000001.10:g.201328356G= , CM000663.1:g.201328356G=	GRCh37
NC_000001.9:g.199594979G=	NCBI36
NG_007556.1:g.23450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.864C=	ENSP00000402238.3:p.Val288=
ENST00000367318.10:c.849C=	ENSP00000356287.5:p.Val283=
ENST00000367322.6:c.837C=	ENSP00000356291.2:p.Val279=
ENST00000412633.3:c.840C=	ENSP00000408731.2:p.Val280=
ENST00000422165.6:c.870C=	ENSP00000395163.2:p.Val290=
ENST00000438742.6:c.828C=	ENSP00000414036.2:p.Val276=
ENST00000651504.1:n.1340C=
ENST00000656932.1:c.879C= MANE Select	ENSP00000499593.1:p.Val293=
ENST00000658476.1:c.914C=	ENSP00000499741.1:p.Ser305=
ENST00000660295.1:c.849C=	ENSP00000499418.1:p.Val283=
ENST00000662159.1:c.*238C=	ENSP00000499796.1:n.*238C=
ENST00000663843.1:c.*779C=	ENSP00000499590.1:n.*779C=
ENST00000666449.1:c.*124C=	ENSP00000499667.1:n.*124C=
ENST00000236918.11:c.879C=	ENSP00000236918.8:p.Val293=
ENST00000360372.8:c.750C=	ENSP00000353535.5:p.Val250=
ENST00000367315.6:c.858C=	ENSP00000356284.3:p.Val286=
ENST00000367317.8:c.831C=	ENSP00000356286.5:p.Val277=
ENST00000367318.9:c.849C=	ENSP00000356287.5:p.Val283=
ENST00000367320.6:c.750C=	ENSP00000356289.2:p.Val250=
ENST00000367322.5:c.840C=	ENSP00000356291.1:p.Val280=
ENST00000421663.6:c.663C=	ENSP00000404134.3:p.Val221=
ENST00000458432.6:c.663C=	ENSP00000387874.3:p.Val221=
ENST00000460780.5:n.1998C=
ENST00000476888.5:n.296C=
ENST00000491504.5:n.2088C=
ENST00000509001.5:c.849C=	ENSP00000422031.1:p.Val283=
NM_000364.3:c.870C=	NP_000355.2:p.Val290=
NM_001001430.2:c.849C=	NP_001001430.1:p.Val283=
NM_001001431.2:c.840C=	NP_001001431.1:p.Val280=
NM_001001432.2:c.831C=	NP_001001432.1:p.Val277=
NM_001276345.1:c.879C=	NP_001263274.1:p.Val293=
NM_001276346.1:c.750C=	NP_001263275.1:p.Val250=
NM_001276347.1:c.849C=	NP_001263276.1:p.Val283=
XM_006711508.2:c.849C=	XP_006711571.1:p.Val283=
XM_006711509.2:c.846C=	XP_006711572.1:p.Val282=
XM_011509938.1:c.879C=	XP_011508240.1:p.Val293=
XM_011509939.1:c.876C=	XP_011508241.1:p.Val292=
XM_011509940.1:c.876C=	XP_011508242.1:p.Val292=
XM_011509941.1:c.873C=	XP_011508243.1:p.Val291=
XM_011509942.1:c.834C=	XP_011508244.1:p.Val278=
XM_011509943.1:c.834C=	XP_011508245.1:p.Val278=
XM_011509944.1:c.831C=	XP_011508246.1:p.Val277=
XM_011509946.1:c.672C=	XP_011508248.1:p.Val224=
XM_006711508.3:c.849C=	XP_006711571.1:p.Val283=
XM_006711509.3:c.846C=	XP_006711572.1:p.Val282=
XM_011509938.2:c.879C=	XP_011508240.1:p.Val293=
XM_011509940.2:c.876C=	XP_011508242.1:p.Val292=
XM_011509941.2:c.873C=	XP_011508243.1:p.Val291=
XM_011509942.2:c.834C=	XP_011508244.1:p.Val278=
XM_011509943.2:c.834C=	XP_011508245.1:p.Val278=
XM_011509944.2:c.831C=	XP_011508246.1:p.Val277=
XM_017002216.2:c.846C=	XP_016857705.1:p.Val282=
XM_017002217.1:c.840C=	XP_016857706.1:p.Val280=
XM_024449450.1:c.879C=	XP_024305218.1:p.Val293=
XM_024449454.1:c.846C=	XP_024305222.1:p.Val282=
XM_024449455.1:c.846C=	XP_024305223.1:p.Val282=
NM_000364.4:c.870C=	NP_000355.2:p.Val290=
NM_001001430.3:c.849C=	NP_001001430.1:p.Val283=
NM_001001431.3:c.840C=	NP_001001431.1:p.Val280=
NM_001001432.3:c.831C=	NP_001001432.1:p.Val277=
NM_001276345.2:c.879C= MANE Select	NP_001263274.1:p.Val293=
NM_001276346.2:c.750C=	NP_001263275.1:p.Val250=
NM_001276347.2:c.849C=	NP_001263276.1:p.Val283=