Canonical Allele Identifier: CA344201872

Gene: TNNT2

Linked Data

• gnomAD v3: 1-201359236-C-T
• gnomAD v4: 1-201359236-C-T
• MyVariant Identifiers: chr1:g.201328364C>T (hg19) ; chr1:g.201359236C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359236C>T , CM000663.2:g.201359236C>T	GRCh38
NC_000001.10:g.201328364C>T , CM000663.1:g.201328364C>T	GRCh37
NC_000001.9:g.199594987C>T	NCBI36
NG_007556.1:g.23442G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.856G>A	ENSP00000402238.3:p.Ala286Thr
ENST00000367318.10:c.841G>A	ENSP00000356287.5:p.Ala281Thr
ENST00000367322.6:c.829G>A	ENSP00000356291.2:p.Ala277Thr
ENST00000412633.3:c.832G>A	ENSP00000408731.2:p.Ala278Thr
ENST00000422165.6:c.862G>A	ENSP00000395163.2:p.Ala288Thr
ENST00000438742.6:c.820G>A	ENSP00000414036.2:p.Ala274Thr
ENST00000651504.1:n.1332G>A
ENST00000656932.1:c.871G>A MANE Select	ENSP00000499593.1:p.Ala291Thr
ENST00000658476.1:c.906G>A	ENSP00000499741.1:p.Arg302=
ENST00000660295.1:c.841G>A	ENSP00000499418.1:p.Ala281Thr
ENST00000662159.1:c.*230G>A	ENSP00000499796.1:n.*230G>A
ENST00000663843.1:c.*771G>A	ENSP00000499590.1:n.*771G>A
ENST00000666449.1:c.*116G>A	ENSP00000499667.1:n.*116G>A
ENST00000236918.11:c.871G>A	ENSP00000236918.8:p.Ala291Thr
ENST00000360372.8:c.742G>A	ENSP00000353535.5:p.Ala248Thr
ENST00000367315.6:c.850G>A	ENSP00000356284.3:p.Ala284Thr
ENST00000367317.8:c.823G>A	ENSP00000356286.5:p.Ala275Thr
ENST00000367318.9:c.841G>A	ENSP00000356287.5:p.Ala281Thr
ENST00000367320.6:c.742G>A	ENSP00000356289.2:p.Ala248Thr
ENST00000367322.5:c.832G>A	ENSP00000356291.1:p.Ala278Thr
ENST00000421663.6:c.655G>A	ENSP00000404134.3:p.Ala219Thr
ENST00000458432.6:c.655G>A	ENSP00000387874.3:p.Ala219Thr
ENST00000460780.5:n.1990G>A
ENST00000476888.5:n.288G>A
ENST00000491504.5:n.2080G>A
ENST00000509001.5:c.841G>A	ENSP00000422031.1:p.Ala281Thr
NM_000364.3:c.862G>A	NP_000355.2:p.Ala288Thr
NM_001001430.2:c.841G>A	NP_001001430.1:p.Ala281Thr
NM_001001431.2:c.832G>A	NP_001001431.1:p.Ala278Thr
NM_001001432.2:c.823G>A	NP_001001432.1:p.Ala275Thr
NM_001276345.1:c.871G>A	NP_001263274.1:p.Ala291Thr
NM_001276346.1:c.742G>A	NP_001263275.1:p.Ala248Thr
NM_001276347.1:c.841G>A	NP_001263276.1:p.Ala281Thr
XM_006711508.2:c.841G>A	XP_006711571.1:p.Ala281Thr
XM_006711509.2:c.838G>A	XP_006711572.1:p.Ala280Thr
XM_011509938.1:c.871G>A	XP_011508240.1:p.Ala291Thr
XM_011509939.1:c.868G>A	XP_011508241.1:p.Ala290Thr
XM_011509940.1:c.868G>A	XP_011508242.1:p.Ala290Thr
XM_011509941.1:c.865G>A	XP_011508243.1:p.Ala289Thr
XM_011509942.1:c.826G>A	XP_011508244.1:p.Ala276Thr
XM_011509943.1:c.826G>A	XP_011508245.1:p.Ala276Thr
XM_011509944.1:c.823G>A	XP_011508246.1:p.Ala275Thr
XM_011509946.1:c.664G>A	XP_011508248.1:p.Ala222Thr
XM_006711508.3:c.841G>A	XP_006711571.1:p.Ala281Thr
XM_006711509.3:c.838G>A	XP_006711572.1:p.Ala280Thr
XM_011509938.2:c.871G>A	XP_011508240.1:p.Ala291Thr
XM_011509940.2:c.868G>A	XP_011508242.1:p.Ala290Thr
XM_011509941.2:c.865G>A	XP_011508243.1:p.Ala289Thr
XM_011509942.2:c.826G>A	XP_011508244.1:p.Ala276Thr
XM_011509943.2:c.826G>A	XP_011508245.1:p.Ala276Thr
XM_011509944.2:c.823G>A	XP_011508246.1:p.Ala275Thr
XM_017002216.2:c.838G>A	XP_016857705.1:p.Ala280Thr
XM_017002217.1:c.832G>A	XP_016857706.1:p.Ala278Thr
XM_024449450.1:c.871G>A	XP_024305218.1:p.Ala291Thr
XM_024449454.1:c.838G>A	XP_024305222.1:p.Ala280Thr
XM_024449455.1:c.838G>A	XP_024305223.1:p.Ala280Thr
NM_000364.4:c.862G>A	NP_000355.2:p.Ala288Thr
NM_001001430.3:c.841G>A	NP_001001430.1:p.Ala281Thr
NM_001001431.3:c.832G>A	NP_001001431.1:p.Ala278Thr
NM_001001432.3:c.823G>A	NP_001001432.1:p.Ala275Thr
NM_001276345.2:c.871G>A MANE Select	NP_001263274.1:p.Ala291Thr
NM_001276346.2:c.742G>A	NP_001263275.1:p.Ala248Thr
NM_001276347.2:c.841G>A	NP_001263276.1:p.Ala281Thr