Canonical Allele Identifier: CA344201859

Gene: TNNT2

Linked Data

• MyVariant Identifiers: chr1:g.201328361T>G (hg19) ; chr1:g.201359233T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359233T>G , CM000663.2:g.201359233T>G	GRCh38
NC_000001.10:g.201328361T>G , CM000663.1:g.201328361T>G	GRCh37
NC_000001.9:g.199594984T>G	NCBI36
NG_007556.1:g.23445A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.859A>C	ENSP00000402238.3:p.Lys287Gln
ENST00000367318.10:c.844A>C	ENSP00000356287.5:p.Lys282Gln
ENST00000367322.6:c.832A>C	ENSP00000356291.2:p.Lys278Gln
ENST00000412633.3:c.835A>C	ENSP00000408731.2:p.Lys279Gln
ENST00000422165.6:c.865A>C	ENSP00000395163.2:p.Lys289Gln
ENST00000438742.6:c.823A>C	ENSP00000414036.2:p.Lys275Gln
ENST00000651504.1:n.1335A>C
ENST00000656932.1:c.874A>C MANE Select	ENSP00000499593.1:p.Lys292Gln
ENST00000658476.1:c.909A>C	ENSP00000499741.1:p.Leu303=
ENST00000660295.1:c.844A>C	ENSP00000499418.1:p.Lys282Gln
ENST00000662159.1:c.*233A>C	ENSP00000499796.1:n.*233A>C
ENST00000663843.1:c.*774A>C	ENSP00000499590.1:n.*774A>C
ENST00000666449.1:c.*119A>C	ENSP00000499667.1:n.*119A>C
ENST00000236918.11:c.874A>C	ENSP00000236918.8:p.Lys292Gln
ENST00000360372.8:c.745A>C	ENSP00000353535.5:p.Lys249Gln
ENST00000367315.6:c.853A>C	ENSP00000356284.3:p.Lys285Gln
ENST00000367317.8:c.826A>C	ENSP00000356286.5:p.Lys276Gln
ENST00000367318.9:c.844A>C	ENSP00000356287.5:p.Lys282Gln
ENST00000367320.6:c.745A>C	ENSP00000356289.2:p.Lys249Gln
ENST00000367322.5:c.835A>C	ENSP00000356291.1:p.Lys279Gln
ENST00000421663.6:c.658A>C	ENSP00000404134.3:p.Lys220Gln
ENST00000458432.6:c.658A>C	ENSP00000387874.3:p.Lys220Gln
ENST00000460780.5:n.1993A>C
ENST00000476888.5:n.291A>C
ENST00000491504.5:n.2083A>C
ENST00000509001.5:c.844A>C	ENSP00000422031.1:p.Lys282Gln
NM_000364.3:c.865A>C	NP_000355.2:p.Lys289Gln
NM_001001430.2:c.844A>C	NP_001001430.1:p.Lys282Gln
NM_001001431.2:c.835A>C	NP_001001431.1:p.Lys279Gln
NM_001001432.2:c.826A>C	NP_001001432.1:p.Lys276Gln
NM_001276345.1:c.874A>C	NP_001263274.1:p.Lys292Gln
NM_001276346.1:c.745A>C	NP_001263275.1:p.Lys249Gln
NM_001276347.1:c.844A>C	NP_001263276.1:p.Lys282Gln
XM_006711508.2:c.844A>C	XP_006711571.1:p.Lys282Gln
XM_006711509.2:c.841A>C	XP_006711572.1:p.Lys281Gln
XM_011509938.1:c.874A>C	XP_011508240.1:p.Lys292Gln
XM_011509939.1:c.871A>C	XP_011508241.1:p.Lys291Gln
XM_011509940.1:c.871A>C	XP_011508242.1:p.Lys291Gln
XM_011509941.1:c.868A>C	XP_011508243.1:p.Lys290Gln
XM_011509942.1:c.829A>C	XP_011508244.1:p.Lys277Gln
XM_011509943.1:c.829A>C	XP_011508245.1:p.Lys277Gln
XM_011509944.1:c.826A>C	XP_011508246.1:p.Lys276Gln
XM_011509946.1:c.667A>C	XP_011508248.1:p.Lys223Gln
XM_006711508.3:c.844A>C	XP_006711571.1:p.Lys282Gln
XM_006711509.3:c.841A>C	XP_006711572.1:p.Lys281Gln
XM_011509938.2:c.874A>C	XP_011508240.1:p.Lys292Gln
XM_011509940.2:c.871A>C	XP_011508242.1:p.Lys291Gln
XM_011509941.2:c.868A>C	XP_011508243.1:p.Lys290Gln
XM_011509942.2:c.829A>C	XP_011508244.1:p.Lys277Gln
XM_011509943.2:c.829A>C	XP_011508245.1:p.Lys277Gln
XM_011509944.2:c.826A>C	XP_011508246.1:p.Lys276Gln
XM_017002216.2:c.841A>C	XP_016857705.1:p.Lys281Gln
XM_017002217.1:c.835A>C	XP_016857706.1:p.Lys279Gln
XM_024449450.1:c.874A>C	XP_024305218.1:p.Lys292Gln
XM_024449454.1:c.841A>C	XP_024305222.1:p.Lys281Gln
XM_024449455.1:c.841A>C	XP_024305223.1:p.Lys281Gln
NM_000364.4:c.865A>C	NP_000355.2:p.Lys289Gln
NM_001001430.3:c.844A>C	NP_001001430.1:p.Lys282Gln
NM_001001431.3:c.835A>C	NP_001001431.1:p.Lys279Gln
NM_001001432.3:c.826A>C	NP_001001432.1:p.Lys276Gln
NM_001276345.2:c.874A>C MANE Select	NP_001263274.1:p.Lys292Gln
NM_001276346.2:c.745A>C	NP_001263275.1:p.Lys249Gln
NM_001276347.2:c.844A>C	NP_001263276.1:p.Lys282Gln