Canonical Allele Identifier: CA1219709408

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359247G= , CM000663.2:g.201359247G=	GRCh38
NC_000001.10:g.201328375G= , CM000663.1:g.201328375G=	GRCh37
NC_000001.9:g.199594998G=	NCBI36
NG_007556.1:g.23431C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.845C=	ENSP00000402238.3:p.Thr282=
ENST00000367318.10:c.830C=	ENSP00000356287.5:p.Thr277=
ENST00000367322.6:c.818C=	ENSP00000356291.2:p.Thr273=
ENST00000412633.3:c.821C=	ENSP00000408731.2:p.Thr274=
ENST00000422165.6:c.851C=	ENSP00000395163.2:p.Thr284=
ENST00000438742.6:c.809C=	ENSP00000414036.2:p.Thr270=
ENST00000651504.1:n.1321C=
ENST00000656932.1:c.860C= MANE Select	ENSP00000499593.1:p.Thr287=
ENST00000658476.1:c.895C=	ENSP00000499741.1:p.Pro299=
ENST00000660295.1:c.830C=	ENSP00000499418.1:p.Thr277=
ENST00000662159.1:c.*219C=	ENSP00000499796.1:n.*219C=
ENST00000663843.1:c.*760C=	ENSP00000499590.1:n.*760C=
ENST00000666449.1:c.*105C=	ENSP00000499667.1:n.*105C=
ENST00000236918.11:c.860C=	ENSP00000236918.8:p.Thr287=
ENST00000360372.8:c.731C=	ENSP00000353535.5:p.Thr244=
ENST00000367315.6:c.839C=	ENSP00000356284.3:p.Thr280=
ENST00000367317.8:c.812C=	ENSP00000356286.5:p.Thr271=
ENST00000367318.9:c.830C=	ENSP00000356287.5:p.Thr277=
ENST00000367320.6:c.731C=	ENSP00000356289.2:p.Thr244=
ENST00000367322.5:c.821C=	ENSP00000356291.1:p.Thr274=
ENST00000421663.6:c.644C=	ENSP00000404134.3:p.Thr215=
ENST00000438742.5:c.812C=	ENSP00000414036.1:p.Thr271=
ENST00000458432.6:c.644C=	ENSP00000387874.3:p.Thr215=
ENST00000460780.5:n.1979C=
ENST00000476888.5:n.277C=
ENST00000491504.5:n.2069C=
ENST00000509001.5:c.830C=	ENSP00000422031.1:p.Thr277=
NM_000364.3:c.851C=	NP_000355.2:p.Thr284=
NM_001001430.2:c.830C=	NP_001001430.1:p.Thr277=
NM_001001431.2:c.821C=	NP_001001431.1:p.Thr274=
NM_001001432.2:c.812C=	NP_001001432.1:p.Thr271=
NM_001276345.1:c.860C=	NP_001263274.1:p.Thr287=
NM_001276346.1:c.731C=	NP_001263275.1:p.Thr244=
NM_001276347.1:c.830C=	NP_001263276.1:p.Thr277=
XM_006711508.2:c.830C=	XP_006711571.1:p.Thr277=
XM_006711509.2:c.827C=	XP_006711572.1:p.Thr276=
XM_011509938.1:c.860C=	XP_011508240.1:p.Thr287=
XM_011509939.1:c.857C=	XP_011508241.1:p.Thr286=
XM_011509940.1:c.857C=	XP_011508242.1:p.Thr286=
XM_011509941.1:c.854C=	XP_011508243.1:p.Thr285=
XM_011509942.1:c.815C=	XP_011508244.1:p.Thr272=
XM_011509943.1:c.815C=	XP_011508245.1:p.Thr272=
XM_011509944.1:c.812C=	XP_011508246.1:p.Thr271=
XM_011509946.1:c.653C=	XP_011508248.1:p.Thr218=
XM_006711508.3:c.830C=	XP_006711571.1:p.Thr277=
XM_006711509.3:c.827C=	XP_006711572.1:p.Thr276=
XM_011509938.2:c.860C=	XP_011508240.1:p.Thr287=
XM_011509940.2:c.857C=	XP_011508242.1:p.Thr286=
XM_011509941.2:c.854C=	XP_011508243.1:p.Thr285=
XM_011509942.2:c.815C=	XP_011508244.1:p.Thr272=
XM_011509943.2:c.815C=	XP_011508245.1:p.Thr272=
XM_011509944.2:c.812C=	XP_011508246.1:p.Thr271=
XM_017002216.2:c.827C=	XP_016857705.1:p.Thr276=
XM_017002217.1:c.821C=	XP_016857706.1:p.Thr274=
XM_024449450.1:c.860C=	XP_024305218.1:p.Thr287=
XM_024449454.1:c.827C=	XP_024305222.1:p.Thr276=
XM_024449455.1:c.827C=	XP_024305223.1:p.Thr276=
NM_000364.4:c.851C=	NP_000355.2:p.Thr284=
NM_001001430.3:c.830C=	NP_001001430.1:p.Thr277=
NM_001001431.3:c.821C=	NP_001001431.1:p.Thr274=
NM_001001432.3:c.812C=	NP_001001432.1:p.Thr271=
NM_001276345.2:c.860C= MANE Select	NP_001263274.1:p.Thr287=
NM_001276346.2:c.731C=	NP_001263275.1:p.Thr244=
NM_001276347.2:c.830C=	NP_001263276.1:p.Thr277=