Canonical Allele Identifier: CA005233

Gene: TNNT2

Linked Data

• ClinVar Variation Id: 181634
• ClinVar RCV Id: RCV000159320 ; RCV001319277 ; RCV003445597 ; RCV003445596 ; RCV003445598
• dbSNP Id: rs730881114
• MyVariant Identifiers: chr1:g.201328384C>A (hg19) ; chr1:g.201359256C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359256C>A , CM000663.2:g.201359256C>A	GRCh38
NC_000001.10:g.201328384C>A , CM000663.1:g.201328384C>A	GRCh37
NC_000001.9:g.199595007C>A	NCBI36
NG_007556.1:g.23422G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.837-1G>T	ENSP00000402238.3:n.837-1G>T
ENST00000367318.10:c.822-1G>T	ENSP00000356287.5:n.822-1G>T
ENST00000367322.6:c.810-1G>T	ENSP00000356291.2:n.810-1G>T
ENST00000412633.3:c.813-1G>T	ENSP00000408731.2:n.813-1G>T
ENST00000422165.6:c.843-1G>T	ENSP00000395163.2:n.843-1G>T
ENST00000438742.6:c.801-1G>T	ENSP00000414036.2:n.801-1G>T
ENST00000651504.1:n.1313-1G>T
ENST00000656932.1:c.852-1G>T MANE Select	ENSP00000499593.1:n.852-1G>T
ENST00000658476.1:c.887-1G>T	ENSP00000499741.1:n.887-1G>T
ENST00000660295.1:c.822-1G>T	ENSP00000499418.1:n.822-1G>T
ENST00000662159.1:c.*211-1G>T	ENSP00000499796.1:n.*211-1G>T
ENST00000663843.1:c.*752-1G>T	ENSP00000499590.1:n.*752-1G>T
ENST00000666449.1:c.*97-1G>T	ENSP00000499667.1:n.*97-1G>T
ENST00000236918.11:c.852-1G>T	ENSP00000236918.8:n.852-1G>T
ENST00000360372.8:c.723-1G>T	ENSP00000353535.5:n.723-1G>T
ENST00000367315.6:c.831-1G>T	ENSP00000356284.3:n.831-1G>T
ENST00000367317.8:c.804-1G>T	ENSP00000356286.5:n.804-1G>T
ENST00000367318.9:c.822-1G>T	ENSP00000356287.5:n.822-1G>T
ENST00000367320.6:c.723-1G>T	ENSP00000356289.2:n.723-1G>T
ENST00000367322.5:c.813-1G>T	ENSP00000356291.1:n.813-1G>T
ENST00000421663.6:c.636-1G>T	ENSP00000404134.3:n.636-1G>T
ENST00000438742.5:c.804-1G>T	ENSP00000414036.1:n.804-1G>T
ENST00000458432.6:c.636-1G>T	ENSP00000387874.3:n.636-1G>T
ENST00000460780.5:n.1971-1G>T
ENST00000476888.5:n.269-1G>T
ENST00000491504.5:n.2061-1G>T
ENST00000509001.5:c.822-1G>T	ENSP00000422031.1:n.822-1G>T
NM_000364.3:c.843-1G>T	NP_000355.2:n.843-1G>T
NM_001001430.2:c.822-1G>T	NP_001001430.1:n.822-1G>T
NM_001001431.2:c.813-1G>T	NP_001001431.1:n.813-1G>T
NM_001001432.2:c.804-1G>T	NP_001001432.1:n.804-1G>T
NM_001276345.1:c.852-1G>T	NP_001263274.1:n.852-1G>T
NM_001276346.1:c.723-1G>T	NP_001263275.1:n.723-1G>T
NM_001276347.1:c.822-1G>T	NP_001263276.1:n.822-1G>T
XM_006711508.2:c.822-1G>T	XP_006711571.1:n.822-1G>T
XM_006711509.2:c.819-1G>T	XP_006711572.1:n.819-1G>T
XM_011509938.1:c.852-1G>T	XP_011508240.1:n.852-1G>T
XM_011509939.1:c.849-1G>T	XP_011508241.1:n.849-1G>T
XM_011509940.1:c.849-1G>T	XP_011508242.1:n.849-1G>T
XM_011509941.1:c.846-1G>T	XP_011508243.1:n.846-1G>T
XM_011509942.1:c.807-1G>T	XP_011508244.1:n.807-1G>T
XM_011509943.1:c.807-1G>T	XP_011508245.1:n.807-1G>T
XM_011509944.1:c.804-1G>T	XP_011508246.1:n.804-1G>T
XM_011509946.1:c.645-1G>T	XP_011508248.1:n.645-1G>T
XM_006711508.3:c.822-1G>T	XP_006711571.1:n.822-1G>T
XM_006711509.3:c.819-1G>T	XP_006711572.1:n.819-1G>T
XM_011509938.2:c.852-1G>T	XP_011508240.1:n.852-1G>T
XM_011509940.2:c.849-1G>T	XP_011508242.1:n.849-1G>T
XM_011509941.2:c.846-1G>T	XP_011508243.1:n.846-1G>T
XM_011509942.2:c.807-1G>T	XP_011508244.1:n.807-1G>T
XM_011509943.2:c.807-1G>T	XP_011508245.1:n.807-1G>T
XM_011509944.2:c.804-1G>T	XP_011508246.1:n.804-1G>T
XM_017002216.2:c.819-1G>T	XP_016857705.1:n.819-1G>T
XM_017002217.1:c.813-1G>T	XP_016857706.1:n.813-1G>T
XM_024449450.1:c.852-1G>T	XP_024305218.1:n.852-1G>T
XM_024449454.1:c.819-1G>T	XP_024305222.1:n.819-1G>T
XM_024449455.1:c.819-1G>T	XP_024305223.1:n.819-1G>T
NM_000364.4:c.843-1G>T	NP_000355.2:n.843-1G>T
NM_001001430.3:c.822-1G>T	NP_001001430.1:n.822-1G>T
NM_001001431.3:c.813-1G>T	NP_001001431.1:n.813-1G>T
NM_001001432.3:c.804-1G>T	NP_001001432.1:n.804-1G>T
NM_001276345.2:c.852-1G>T MANE Select	NP_001263274.1:n.852-1G>T
NM_001276346.2:c.723-1G>T	NP_001263275.1:n.723-1G>T
NM_001276347.2:c.822-1G>T	NP_001263276.1:n.822-1G>T