Canonical Allele Identifier: CA528090151

Gene: TNNT2

Linked Data

• ClinVar Variation Id: 488163
• ClinVar RCV Id: RCV000578021 ; RCV000578056 ; RCV000577941
• dbSNP Id: rs193922620
• gnomAD v2: 1-201328746-C-G
• gnomAD v4: 1-201359618-C-G
• MyVariant Identifiers: chr1:g.201328746C>G (hg19) ; chr1:g.201359618C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359618C>G , CM000663.2:g.201359618C>G	GRCh38
NC_000001.10:g.201328746C>G , CM000663.1:g.201328746C>G	GRCh37
NC_000001.9:g.199595369C>G	NCBI36
NG_007556.1:g.23060G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.836+5G>C	ENSP00000402238.3:n.836+5G>C
ENST00000367318.10:c.821+5G>C	ENSP00000356287.5:n.821+5G>C
ENST00000367322.6:c.809+5G>C	ENSP00000356291.2:n.809+5G>C
ENST00000412633.3:c.812+5G>C	ENSP00000408731.2:n.812+5G>C
ENST00000422165.6:c.842+5G>C	ENSP00000395163.2:n.842+5G>C
ENST00000438742.6:c.800+5G>C	ENSP00000414036.2:n.800+5G>C
ENST00000651504.1:n.1312+5G>C
ENST00000656932.1:c.851+5G>C MANE Select	ENSP00000499593.1:n.851+5G>C
ENST00000658476.1:c.886+5G>C	ENSP00000499741.1:n.886+5G>C
ENST00000660295.1:c.821+5G>C	ENSP00000499418.1:n.821+5G>C
ENST00000662159.1:c.*210+5G>C	ENSP00000499796.1:n.*210+5G>C
ENST00000663843.1:c.*751+5G>C	ENSP00000499590.1:n.*751+5G>C
ENST00000666449.1:c.*96+5G>C	ENSP00000499667.1:n.*96+5G>C
ENST00000236918.11:c.851+5G>C	ENSP00000236918.8:n.851+5G>C
ENST00000360372.8:c.722+5G>C	ENSP00000353535.5:n.722+5G>C
ENST00000367315.6:c.830+5G>C	ENSP00000356284.3:n.830+5G>C
ENST00000367317.8:c.803+5G>C	ENSP00000356286.5:n.803+5G>C
ENST00000367318.9:c.821+5G>C	ENSP00000356287.5:n.821+5G>C
ENST00000367320.6:c.722+5G>C	ENSP00000356289.2:n.722+5G>C
ENST00000367322.5:c.812+5G>C	ENSP00000356291.1:n.812+5G>C
ENST00000421663.6:c.635+5G>C	ENSP00000404134.3:n.635+5G>C
ENST00000438742.5:c.803+5G>C	ENSP00000414036.1:n.803+5G>C
ENST00000458432.6:c.635+5G>C	ENSP00000387874.3:n.635+5G>C
ENST00000460780.5:n.1970+5G>C
ENST00000476888.5:n.268+5G>C
ENST00000491504.5:n.2060+5G>C
ENST00000509001.5:c.821+5G>C	ENSP00000422031.1:n.821+5G>C
NM_000364.3:c.842+5G>C	NP_000355.2:n.842+5G>C
NM_001001430.2:c.821+5G>C	NP_001001430.1:n.821+5G>C
NM_001001431.2:c.812+5G>C	NP_001001431.1:n.812+5G>C
NM_001001432.2:c.803+5G>C	NP_001001432.1:n.803+5G>C
NM_001276345.1:c.851+5G>C	NP_001263274.1:n.851+5G>C
NM_001276346.1:c.722+5G>C	NP_001263275.1:n.722+5G>C
NM_001276347.1:c.821+5G>C	NP_001263276.1:n.821+5G>C
XM_006711508.2:c.821+5G>C	XP_006711571.1:n.821+5G>C
XM_006711509.2:c.818+5G>C	XP_006711572.1:n.818+5G>C
XM_011509938.1:c.851+5G>C	XP_011508240.1:n.851+5G>C
XM_011509939.1:c.848+5G>C	XP_011508241.1:n.848+5G>C
XM_011509940.1:c.848+5G>C	XP_011508242.1:n.848+5G>C
XM_011509941.1:c.845+5G>C	XP_011508243.1:n.845+5G>C
XM_011509942.1:c.806+5G>C	XP_011508244.1:n.806+5G>C
XM_011509943.1:c.806+5G>C	XP_011508245.1:n.806+5G>C
XM_011509944.1:c.803+5G>C	XP_011508246.1:n.803+5G>C
XM_011509946.1:c.644+5G>C	XP_011508248.1:n.644+5G>C
XM_006711508.3:c.821+5G>C	XP_006711571.1:n.821+5G>C
XM_006711509.3:c.818+5G>C	XP_006711572.1:n.818+5G>C
XM_011509938.2:c.851+5G>C	XP_011508240.1:n.851+5G>C
XM_011509940.2:c.848+5G>C	XP_011508242.1:n.848+5G>C
XM_011509941.2:c.845+5G>C	XP_011508243.1:n.845+5G>C
XM_011509942.2:c.806+5G>C	XP_011508244.1:n.806+5G>C
XM_011509943.2:c.806+5G>C	XP_011508245.1:n.806+5G>C
XM_011509944.2:c.803+5G>C	XP_011508246.1:n.803+5G>C
XM_017002216.2:c.818+5G>C	XP_016857705.1:n.818+5G>C
XM_017002217.1:c.812+5G>C	XP_016857706.1:n.812+5G>C
XM_024449450.1:c.851+5G>C	XP_024305218.1:n.851+5G>C
XM_024449454.1:c.818+5G>C	XP_024305222.1:n.818+5G>C
XM_024449455.1:c.818+5G>C	XP_024305223.1:n.818+5G>C
NM_000364.4:c.842+5G>C	NP_000355.2:n.842+5G>C
NM_001001430.3:c.821+5G>C	NP_001001430.1:n.821+5G>C
NM_001001431.3:c.812+5G>C	NP_001001431.1:n.812+5G>C
NM_001001432.3:c.803+5G>C	NP_001001432.1:n.803+5G>C
NM_001276345.2:c.851+5G>C MANE Select	NP_001263274.1:n.851+5G>C
NM_001276346.2:c.722+5G>C	NP_001263275.1:n.722+5G>C
NM_001276347.2:c.821+5G>C	NP_001263276.1:n.821+5G>C