Canonical Allele Identifier: CA730118530

Gene: TNNT2

Linked Data

• dbSNP Id: rs1161217674
• gnomAD v4: 1-201359069-AG-A
• MyVariant Identifiers: chr1:g.201328198del (hg19) ; chr1:g.201359070del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359070del , CM000663.2:g.201359070del	GRCh38
NC_000001.10:g.201328198del , CM000663.1:g.201328198del	GRCh37
NC_000001.9:g.199594821del	NCBI36
NG_007556.1:g.23608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.*140del	ENSP00000402238.3:n.*140del
ENST00000367318.10:c.*140del	ENSP00000356287.5:n.*140del
ENST00000367322.6:c.*140del	ENSP00000356291.2:n.*140del
ENST00000412633.3:c.*140del	ENSP00000408731.2:n.*140del
ENST00000422165.6:c.*140del	ENSP00000395163.2:n.*140del
ENST00000438742.6:c.*140del	ENSP00000414036.2:n.*140del
ENST00000656932.1:c.*140del MANE Select	ENSP00000499593.1:n.*140del
ENST00000658476.1:c.1072del	ENSP00000499741.1:p.Leu358SerfsTer?
ENST00000660295.1:c.*140del	ENSP00000499418.1:n.*140del
ENST00000662159.1:c.*396del	ENSP00000499796.1:n.*396del
ENST00000663843.1:c.*937del	ENSP00000499590.1:n.*937del
ENST00000666449.1:c.*282del	ENSP00000499667.1:n.*282del
ENST00000236918.11:c.1037del	ENSP00000236918.8:n.1037del
ENST00000360372.8:c.908del	ENSP00000353535.5:n.908del
ENST00000367315.6:c.*140del	ENSP00000356284.3:n.*140del
ENST00000367317.8:c.989del	ENSP00000356286.5:n.989del
ENST00000367318.9:c.*140del	ENSP00000356287.5:n.*140del
ENST00000367320.6:c.*140del	ENSP00000356289.2:n.*140del
ENST00000367322.5:c.*140del	ENSP00000356291.1:n.*140del
ENST00000421663.6:c.*140del	ENSP00000404134.3:n.*140del
ENST00000458432.6:c.*140del	ENSP00000387874.3:n.*140del
ENST00000460780.5:n.2156del
ENST00000476888.5:n.454del
ENST00000491504.5:n.2246del
ENST00000509001.5:c.*140del	ENSP00000422031.1:n.*140del
NM_000364.3:c.*140del	NP_000355.2:n.*140del
NM_001001430.2:c.*140del	NP_001001430.1:n.*140del
NM_001001431.2:c.*140del	NP_001001431.1:n.*140del
NM_001001432.2:c.*140del	NP_001001432.1:n.*140del
NM_001276345.1:c.*140del	NP_001263274.1:n.*140del
NM_001276346.1:c.*140del	NP_001263275.1:n.*140del
NM_001276347.1:c.*140del	NP_001263276.1:n.*140del
XM_006711508.2:c.*140del	XP_006711571.1:n.*140del
XM_006711509.2:c.*140del	XP_006711572.1:n.*140del
XM_011509938.1:c.*140del	XP_011508240.1:n.*140del
XM_011509939.1:c.*140del	XP_011508241.1:n.*140del
XM_011509940.1:c.*140del	XP_011508242.1:n.*140del
XM_011509941.1:c.*140del	XP_011508243.1:n.*140del
XM_011509942.1:c.*140del	XP_011508244.1:n.*140del
XM_011509943.1:c.*140del	XP_011508245.1:n.*140del
XM_011509944.1:c.*140del	XP_011508246.1:n.*140del
XM_011509946.1:c.*140del	XP_011508248.1:n.*140del
XM_006711508.3:c.*140del	XP_006711571.1:n.*140del
XM_006711509.3:c.*140del	XP_006711572.1:n.*140del
XM_011509938.2:c.*140del	XP_011508240.1:n.*140del
XM_011509940.2:c.*140del	XP_011508242.1:n.*140del
XM_011509941.2:c.*140del	XP_011508243.1:n.*140del
XM_011509942.2:c.*140del	XP_011508244.1:n.*140del
XM_011509943.2:c.*140del	XP_011508245.1:n.*140del
XM_011509944.2:c.*140del	XP_011508246.1:n.*140del
XM_017002216.2:c.*140del	XP_016857705.1:n.*140del
XM_017002217.1:c.*140del	XP_016857706.1:n.*140del
XM_024449450.1:c.*140del	XP_024305218.1:n.*140del
XM_024449454.1:c.*140del	XP_024305222.1:n.*140del
XM_024449455.1:c.*140del	XP_024305223.1:n.*140del
NM_000364.4:c.*140del	NP_000355.2:n.*140del
NM_001001430.3:c.*140del	NP_001001430.1:n.*140del
NM_001001431.3:c.*140del	NP_001001431.1:n.*140del
NM_001001432.3:c.*140del	NP_001001432.1:n.*140del
NM_001276345.2:c.*140del MANE Select	NP_001263274.1:n.*140del
NM_001276346.2:c.*140del	NP_001263275.1:n.*140del
NM_001276347.2:c.*140del	NP_001263276.1:n.*140del