Canonical Allele Identifier: CA005165

Gene: TNNT2

Linked Data

• ClinVar Variation Id: 181648
• ClinVar RCV Id: RCV000159345
• dbSNP Id: rs4523540
• MyVariant Identifiers: chr1:g.201328767T>A (hg19) ; chr1:g.201359639T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.820A>T	ENSP00000402238.3:p.Asn274Tyr
ENST00000367318.10:c.805A>T	ENSP00000356287.5:p.Asn269Tyr
ENST00000367322.6:c.793A>T	ENSP00000356291.2:p.Asn265Tyr
ENST00000412633.3:c.796A>T	ENSP00000408731.2:p.Asn266Tyr
ENST00000422165.6:c.826A>T	ENSP00000395163.2:p.Asn276Tyr
ENST00000438742.6:c.784A>T	ENSP00000414036.2:p.Asn262Tyr
ENST00000651504.1:n.1296A>T
ENST00000656932.1:c.835A>T MANE Select	ENSP00000499593.1:p.Asn279Tyr
ENST00000658476.1:c.870A>T	ENSP00000499741.1:p.Ser290=
ENST00000660295.1:c.805A>T	ENSP00000499418.1:p.Asn269Tyr
ENST00000662159.1:c.*194A>T	ENSP00000499796.1:n.*194A>T
ENST00000663843.1:c.*735A>T	ENSP00000499590.1:n.*735A>T
ENST00000666449.1:c.*80A>T	ENSP00000499667.1:n.*80A>T
ENST00000236918.11:c.835A>T	ENSP00000236918.8:p.Asn279Tyr
ENST00000360372.8:c.706A>T	ENSP00000353535.5:p.Asn236Tyr
ENST00000367315.6:c.814A>T	ENSP00000356284.3:p.Asn272Tyr
ENST00000367317.8:c.787A>T	ENSP00000356286.5:p.Asn263Tyr
ENST00000367318.9:c.805A>T	ENSP00000356287.5:p.Asn269Tyr
ENST00000367320.6:c.706A>T	ENSP00000356289.2:p.Asn236Tyr
ENST00000367322.5:c.796A>T	ENSP00000356291.1:p.Asn266Tyr
ENST00000421663.6:c.619A>T	ENSP00000404134.3:p.Asn207Tyr
ENST00000438742.5:c.787A>T	ENSP00000414036.1:p.Asn263Tyr
ENST00000458432.6:c.619A>T	ENSP00000387874.3:p.Asn207Tyr
ENST00000460780.5:n.1954A>T
ENST00000476888.5:n.252A>T
ENST00000491504.5:n.2044A>T
ENST00000509001.5:c.805A>T	ENSP00000422031.1:p.Asn269Tyr
NM_000364.3:c.826A>T	NP_000355.2:p.Asn276Tyr
NM_001001430.2:c.805A>T	NP_001001430.1:p.Asn269Tyr
NM_001001431.2:c.796A>T	NP_001001431.1:p.Asn266Tyr
NM_001001432.2:c.787A>T	NP_001001432.1:p.Asn263Tyr
NM_001276345.1:c.835A>T	NP_001263274.1:p.Asn279Tyr
NM_001276346.1:c.706A>T	NP_001263275.1:p.Asn236Tyr
NM_001276347.1:c.805A>T	NP_001263276.1:p.Asn269Tyr
XM_006711508.2:c.805A>T	XP_006711571.1:p.Asn269Tyr
XM_006711509.2:c.802A>T	XP_006711572.1:p.Asn268Tyr
XM_011509938.1:c.835A>T	XP_011508240.1:p.Asn279Tyr
XM_011509939.1:c.832A>T	XP_011508241.1:p.Asn278Tyr
XM_011509940.1:c.832A>T	XP_011508242.1:p.Asn278Tyr
XM_011509941.1:c.829A>T	XP_011508243.1:p.Asn277Tyr
XM_011509942.1:c.790A>T	XP_011508244.1:p.Asn264Tyr
XM_011509943.1:c.790A>T	XP_011508245.1:p.Asn264Tyr
XM_011509944.1:c.787A>T	XP_011508246.1:p.Asn263Tyr
XM_011509946.1:c.628A>T	XP_011508248.1:p.Asn210Tyr
XM_006711508.3:c.805A>T	XP_006711571.1:p.Asn269Tyr
XM_006711509.3:c.802A>T	XP_006711572.1:p.Asn268Tyr
XM_011509938.2:c.835A>T	XP_011508240.1:p.Asn279Tyr
XM_011509940.2:c.832A>T	XP_011508242.1:p.Asn278Tyr
XM_011509941.2:c.829A>T	XP_011508243.1:p.Asn277Tyr
XM_011509942.2:c.790A>T	XP_011508244.1:p.Asn264Tyr
XM_011509943.2:c.790A>T	XP_011508245.1:p.Asn264Tyr
XM_011509944.2:c.787A>T	XP_011508246.1:p.Asn263Tyr
XM_017002216.2:c.802A>T	XP_016857705.1:p.Asn268Tyr
XM_017002217.1:c.796A>T	XP_016857706.1:p.Asn266Tyr
XM_024449450.1:c.835A>T	XP_024305218.1:p.Asn279Tyr
XM_024449454.1:c.802A>T	XP_024305222.1:p.Asn268Tyr
XM_024449455.1:c.802A>T	XP_024305223.1:p.Asn268Tyr
NM_000364.4:c.826A>T	NP_000355.2:p.Asn276Tyr
NM_001001430.3:c.805A>T	NP_001001430.1:p.Asn269Tyr
NM_001001431.3:c.796A>T	NP_001001431.1:p.Asn266Tyr
NM_001001432.3:c.787A>T	NP_001001432.1:p.Asn263Tyr
NM_001276345.2:c.835A>T MANE Select	NP_001263274.1:p.Asn279Tyr
NM_001276346.2:c.706A>T	NP_001263275.1:p.Asn236Tyr
NM_001276347.2:c.805A>T	NP_001263276.1:p.Asn269Tyr