Canonical Allele Identifier: CA344201867

Gene: TNNT2

Linked Data

• MyVariant Identifiers: chr1:g.201328363G>T (hg19) ; chr1:g.201359235G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359235G>T , CM000663.2:g.201359235G>T	GRCh38
NC_000001.10:g.201328363G>T , CM000663.1:g.201328363G>T	GRCh37
NC_000001.9:g.199594986G>T	NCBI36
NG_007556.1:g.23443C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.857C>A	ENSP00000402238.3:p.Ala286Asp
ENST00000367318.10:c.842C>A	ENSP00000356287.5:p.Ala281Asp
ENST00000367322.6:c.830C>A	ENSP00000356291.2:p.Ala277Asp
ENST00000412633.3:c.833C>A	ENSP00000408731.2:p.Ala278Asp
ENST00000422165.6:c.863C>A	ENSP00000395163.2:p.Ala288Asp
ENST00000438742.6:c.821C>A	ENSP00000414036.2:p.Ala274Asp
ENST00000651504.1:n.1333C>A
ENST00000656932.1:c.872C>A MANE Select	ENSP00000499593.1:p.Ala291Asp
ENST00000658476.1:c.907C>A	ENSP00000499741.1:p.Leu303Ile
ENST00000660295.1:c.842C>A	ENSP00000499418.1:p.Ala281Asp
ENST00000662159.1:c.*231C>A	ENSP00000499796.1:n.*231C>A
ENST00000663843.1:c.*772C>A	ENSP00000499590.1:n.*772C>A
ENST00000666449.1:c.*117C>A	ENSP00000499667.1:n.*117C>A
ENST00000236918.11:c.872C>A	ENSP00000236918.8:p.Ala291Asp
ENST00000360372.8:c.743C>A	ENSP00000353535.5:p.Ala248Asp
ENST00000367315.6:c.851C>A	ENSP00000356284.3:p.Ala284Asp
ENST00000367317.8:c.824C>A	ENSP00000356286.5:p.Ala275Asp
ENST00000367318.9:c.842C>A	ENSP00000356287.5:p.Ala281Asp
ENST00000367320.6:c.743C>A	ENSP00000356289.2:p.Ala248Asp
ENST00000367322.5:c.833C>A	ENSP00000356291.1:p.Ala278Asp
ENST00000421663.6:c.656C>A	ENSP00000404134.3:p.Ala219Asp
ENST00000458432.6:c.656C>A	ENSP00000387874.3:p.Ala219Asp
ENST00000460780.5:n.1991C>A
ENST00000476888.5:n.289C>A
ENST00000491504.5:n.2081C>A
ENST00000509001.5:c.842C>A	ENSP00000422031.1:p.Ala281Asp
NM_000364.3:c.863C>A	NP_000355.2:p.Ala288Asp
NM_001001430.2:c.842C>A	NP_001001430.1:p.Ala281Asp
NM_001001431.2:c.833C>A	NP_001001431.1:p.Ala278Asp
NM_001001432.2:c.824C>A	NP_001001432.1:p.Ala275Asp
NM_001276345.1:c.872C>A	NP_001263274.1:p.Ala291Asp
NM_001276346.1:c.743C>A	NP_001263275.1:p.Ala248Asp
NM_001276347.1:c.842C>A	NP_001263276.1:p.Ala281Asp
XM_006711508.2:c.842C>A	XP_006711571.1:p.Ala281Asp
XM_006711509.2:c.839C>A	XP_006711572.1:p.Ala280Asp
XM_011509938.1:c.872C>A	XP_011508240.1:p.Ala291Asp
XM_011509939.1:c.869C>A	XP_011508241.1:p.Ala290Asp
XM_011509940.1:c.869C>A	XP_011508242.1:p.Ala290Asp
XM_011509941.1:c.866C>A	XP_011508243.1:p.Ala289Asp
XM_011509942.1:c.827C>A	XP_011508244.1:p.Ala276Asp
XM_011509943.1:c.827C>A	XP_011508245.1:p.Ala276Asp
XM_011509944.1:c.824C>A	XP_011508246.1:p.Ala275Asp
XM_011509946.1:c.665C>A	XP_011508248.1:p.Ala222Asp
XM_006711508.3:c.842C>A	XP_006711571.1:p.Ala281Asp
XM_006711509.3:c.839C>A	XP_006711572.1:p.Ala280Asp
XM_011509938.2:c.872C>A	XP_011508240.1:p.Ala291Asp
XM_011509940.2:c.869C>A	XP_011508242.1:p.Ala290Asp
XM_011509941.2:c.866C>A	XP_011508243.1:p.Ala289Asp
XM_011509942.2:c.827C>A	XP_011508244.1:p.Ala276Asp
XM_011509943.2:c.827C>A	XP_011508245.1:p.Ala276Asp
XM_011509944.2:c.824C>A	XP_011508246.1:p.Ala275Asp
XM_017002216.2:c.839C>A	XP_016857705.1:p.Ala280Asp
XM_017002217.1:c.833C>A	XP_016857706.1:p.Ala278Asp
XM_024449450.1:c.872C>A	XP_024305218.1:p.Ala291Asp
XM_024449454.1:c.839C>A	XP_024305222.1:p.Ala280Asp
XM_024449455.1:c.839C>A	XP_024305223.1:p.Ala280Asp
NM_000364.4:c.863C>A	NP_000355.2:p.Ala288Asp
NM_001001430.3:c.842C>A	NP_001001430.1:p.Ala281Asp
NM_001001431.3:c.833C>A	NP_001001431.1:p.Ala278Asp
NM_001001432.3:c.824C>A	NP_001001432.1:p.Ala275Asp
NM_001276345.2:c.872C>A MANE Select	NP_001263274.1:p.Ala291Asp
NM_001276346.2:c.743C>A	NP_001263275.1:p.Ala248Asp
NM_001276347.2:c.842C>A	NP_001263276.1:p.Ala281Asp