Canonical Allele Identifier: CA088463

Gene: TNNT2

Linked Data

• MyVariant Identifiers: chr1:g.201328360T>C (hg19) ; chr1:g.201359232T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359232T>C , CM000663.2:g.201359232T>C	GRCh38
NC_000001.10:g.201328360T>C , CM000663.1:g.201328360T>C	GRCh37
NC_000001.9:g.199594983T>C	NCBI36
NG_007556.1:g.23446A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.860A>G	ENSP00000402238.3:p.Lys287Arg
ENST00000367318.10:c.845A>G	ENSP00000356287.5:p.Lys282Arg
ENST00000367322.6:c.833A>G	ENSP00000356291.2:p.Lys278Arg
ENST00000412633.3:c.836A>G	ENSP00000408731.2:p.Lys279Arg
ENST00000422165.6:c.866A>G	ENSP00000395163.2:p.Lys289Arg
ENST00000438742.6:c.824A>G	ENSP00000414036.2:p.Lys275Arg
ENST00000651504.1:n.1336A>G
ENST00000656932.1:c.875A>G MANE Select	ENSP00000499593.1:p.Lys292Arg
ENST00000658476.1:c.910A>G	ENSP00000499741.1:p.Lys304Glu
ENST00000660295.1:c.845A>G	ENSP00000499418.1:p.Lys282Arg
ENST00000662159.1:c.*234A>G	ENSP00000499796.1:n.*234A>G
ENST00000663843.1:c.*775A>G	ENSP00000499590.1:n.*775A>G
ENST00000666449.1:c.*120A>G	ENSP00000499667.1:n.*120A>G
ENST00000236918.11:c.875A>G	ENSP00000236918.8:p.Lys292Arg
ENST00000360372.8:c.746A>G	ENSP00000353535.5:p.Lys249Arg
ENST00000367315.6:c.854A>G	ENSP00000356284.3:p.Lys285Arg
ENST00000367317.8:c.827A>G	ENSP00000356286.5:p.Lys276Arg
ENST00000367318.9:c.845A>G	ENSP00000356287.5:p.Lys282Arg
ENST00000367320.6:c.746A>G	ENSP00000356289.2:p.Lys249Arg
ENST00000367322.5:c.836A>G	ENSP00000356291.1:p.Lys279Arg
ENST00000421663.6:c.659A>G	ENSP00000404134.3:p.Lys220Arg
ENST00000458432.6:c.659A>G	ENSP00000387874.3:p.Lys220Arg
ENST00000460780.5:n.1994A>G
ENST00000476888.5:n.292A>G
ENST00000491504.5:n.2084A>G
ENST00000509001.5:c.845A>G	ENSP00000422031.1:p.Lys282Arg
NM_000364.3:c.866A>G	NP_000355.2:p.Lys289Arg
NM_001001430.2:c.845A>G	NP_001001430.1:p.Lys282Arg
NM_001001431.2:c.836A>G	NP_001001431.1:p.Lys279Arg
NM_001001432.2:c.827A>G	NP_001001432.1:p.Lys276Arg
NM_001276345.1:c.875A>G	NP_001263274.1:p.Lys292Arg
NM_001276346.1:c.746A>G	NP_001263275.1:p.Lys249Arg
NM_001276347.1:c.845A>G	NP_001263276.1:p.Lys282Arg
XM_006711508.2:c.845A>G	XP_006711571.1:p.Lys282Arg
XM_006711509.2:c.842A>G	XP_006711572.1:p.Lys281Arg
XM_011509938.1:c.875A>G	XP_011508240.1:p.Lys292Arg
XM_011509939.1:c.872A>G	XP_011508241.1:p.Lys291Arg
XM_011509940.1:c.872A>G	XP_011508242.1:p.Lys291Arg
XM_011509941.1:c.869A>G	XP_011508243.1:p.Lys290Arg
XM_011509942.1:c.830A>G	XP_011508244.1:p.Lys277Arg
XM_011509943.1:c.830A>G	XP_011508245.1:p.Lys277Arg
XM_011509944.1:c.827A>G	XP_011508246.1:p.Lys276Arg
XM_011509946.1:c.668A>G	XP_011508248.1:p.Lys223Arg
XM_006711508.3:c.845A>G	XP_006711571.1:p.Lys282Arg
XM_006711509.3:c.842A>G	XP_006711572.1:p.Lys281Arg
XM_011509938.2:c.875A>G	XP_011508240.1:p.Lys292Arg
XM_011509940.2:c.872A>G	XP_011508242.1:p.Lys291Arg
XM_011509941.2:c.869A>G	XP_011508243.1:p.Lys290Arg
XM_011509942.2:c.830A>G	XP_011508244.1:p.Lys277Arg
XM_011509943.2:c.830A>G	XP_011508245.1:p.Lys277Arg
XM_011509944.2:c.827A>G	XP_011508246.1:p.Lys276Arg
XM_017002216.2:c.842A>G	XP_016857705.1:p.Lys281Arg
XM_017002217.1:c.836A>G	XP_016857706.1:p.Lys279Arg
XM_024449450.1:c.875A>G	XP_024305218.1:p.Lys292Arg
XM_024449454.1:c.842A>G	XP_024305222.1:p.Lys281Arg
XM_024449455.1:c.842A>G	XP_024305223.1:p.Lys281Arg
NM_000364.4:c.866A>G	NP_000355.2:p.Lys289Arg
NM_001001430.3:c.845A>G	NP_001001430.1:p.Lys282Arg
NM_001001431.3:c.836A>G	NP_001001431.1:p.Lys279Arg
NM_001001432.3:c.827A>G	NP_001001432.1:p.Lys276Arg
NM_001276345.2:c.875A>G MANE Select	NP_001263274.1:p.Lys292Arg
NM_001276346.2:c.746A>G	NP_001263275.1:p.Lys249Arg
NM_001276347.2:c.845A>G	NP_001263276.1:p.Lys282Arg