Canonical Allele Identifier: CA344201909

Gene: TNNT2

Linked Data

• MyVariant Identifiers: chr1:g.201328376T>A (hg19) ; chr1:g.201359248T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359248T>A , CM000663.2:g.201359248T>A	GRCh38
NC_000001.10:g.201328376T>A , CM000663.1:g.201328376T>A	GRCh37
NC_000001.9:g.199594999T>A	NCBI36
NG_007556.1:g.23430A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.844A>T	ENSP00000402238.3:p.Thr282Ser
ENST00000367318.10:c.829A>T	ENSP00000356287.5:p.Thr277Ser
ENST00000367322.6:c.817A>T	ENSP00000356291.2:p.Thr273Ser
ENST00000412633.3:c.820A>T	ENSP00000408731.2:p.Thr274Ser
ENST00000422165.6:c.850A>T	ENSP00000395163.2:p.Thr284Ser
ENST00000438742.6:c.808A>T	ENSP00000414036.2:p.Thr270Ser
ENST00000651504.1:n.1320A>T
ENST00000656932.1:c.859A>T MANE Select	ENSP00000499593.1:p.Thr287Ser
ENST00000658476.1:c.894A>T	ENSP00000499741.1:p.Arg298Ser
ENST00000660295.1:c.829A>T	ENSP00000499418.1:p.Thr277Ser
ENST00000662159.1:c.*218A>T	ENSP00000499796.1:n.*218A>T
ENST00000663843.1:c.*759A>T	ENSP00000499590.1:n.*759A>T
ENST00000666449.1:c.*104A>T	ENSP00000499667.1:n.*104A>T
ENST00000236918.11:c.859A>T	ENSP00000236918.8:p.Thr287Ser
ENST00000360372.8:c.730A>T	ENSP00000353535.5:p.Thr244Ser
ENST00000367315.6:c.838A>T	ENSP00000356284.3:p.Thr280Ser
ENST00000367317.8:c.811A>T	ENSP00000356286.5:p.Thr271Ser
ENST00000367318.9:c.829A>T	ENSP00000356287.5:p.Thr277Ser
ENST00000367320.6:c.730A>T	ENSP00000356289.2:p.Thr244Ser
ENST00000367322.5:c.820A>T	ENSP00000356291.1:p.Thr274Ser
ENST00000421663.6:c.643A>T	ENSP00000404134.3:p.Thr215Ser
ENST00000438742.5:c.811A>T	ENSP00000414036.1:p.Thr271Ser
ENST00000458432.6:c.643A>T	ENSP00000387874.3:p.Thr215Ser
ENST00000460780.5:n.1978A>T
ENST00000476888.5:n.276A>T
ENST00000491504.5:n.2068A>T
ENST00000509001.5:c.829A>T	ENSP00000422031.1:p.Thr277Ser
NM_000364.3:c.850A>T	NP_000355.2:p.Thr284Ser
NM_001001430.2:c.829A>T	NP_001001430.1:p.Thr277Ser
NM_001001431.2:c.820A>T	NP_001001431.1:p.Thr274Ser
NM_001001432.2:c.811A>T	NP_001001432.1:p.Thr271Ser
NM_001276345.1:c.859A>T	NP_001263274.1:p.Thr287Ser
NM_001276346.1:c.730A>T	NP_001263275.1:p.Thr244Ser
NM_001276347.1:c.829A>T	NP_001263276.1:p.Thr277Ser
XM_006711508.2:c.829A>T	XP_006711571.1:p.Thr277Ser
XM_006711509.2:c.826A>T	XP_006711572.1:p.Thr276Ser
XM_011509938.1:c.859A>T	XP_011508240.1:p.Thr287Ser
XM_011509939.1:c.856A>T	XP_011508241.1:p.Thr286Ser
XM_011509940.1:c.856A>T	XP_011508242.1:p.Thr286Ser
XM_011509941.1:c.853A>T	XP_011508243.1:p.Thr285Ser
XM_011509942.1:c.814A>T	XP_011508244.1:p.Thr272Ser
XM_011509943.1:c.814A>T	XP_011508245.1:p.Thr272Ser
XM_011509944.1:c.811A>T	XP_011508246.1:p.Thr271Ser
XM_011509946.1:c.652A>T	XP_011508248.1:p.Thr218Ser
XM_006711508.3:c.829A>T	XP_006711571.1:p.Thr277Ser
XM_006711509.3:c.826A>T	XP_006711572.1:p.Thr276Ser
XM_011509938.2:c.859A>T	XP_011508240.1:p.Thr287Ser
XM_011509940.2:c.856A>T	XP_011508242.1:p.Thr286Ser
XM_011509941.2:c.853A>T	XP_011508243.1:p.Thr285Ser
XM_011509942.2:c.814A>T	XP_011508244.1:p.Thr272Ser
XM_011509943.2:c.814A>T	XP_011508245.1:p.Thr272Ser
XM_011509944.2:c.811A>T	XP_011508246.1:p.Thr271Ser
XM_017002216.2:c.826A>T	XP_016857705.1:p.Thr276Ser
XM_017002217.1:c.820A>T	XP_016857706.1:p.Thr274Ser
XM_024449450.1:c.859A>T	XP_024305218.1:p.Thr287Ser
XM_024449454.1:c.826A>T	XP_024305222.1:p.Thr276Ser
XM_024449455.1:c.826A>T	XP_024305223.1:p.Thr276Ser
NM_000364.4:c.850A>T	NP_000355.2:p.Thr284Ser
NM_001001430.3:c.829A>T	NP_001001430.1:p.Thr277Ser
NM_001001431.3:c.820A>T	NP_001001431.1:p.Thr274Ser
NM_001001432.3:c.811A>T	NP_001001432.1:p.Thr271Ser
NM_001276345.2:c.859A>T MANE Select	NP_001263274.1:p.Thr287Ser
NM_001276346.2:c.730A>T	NP_001263275.1:p.Thr244Ser
NM_001276347.2:c.829A>T	NP_001263276.1:p.Thr277Ser