Canonical Allele Identifier: CA090115

Gene: TNNT2

Linked Data

• MyVariant Identifiers: chr1:g.201328358C>A (hg19) ; chr1:g.201359230C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359230C>A , CM000663.2:g.201359230C>A	GRCh38
NC_000001.10:g.201328358C>A , CM000663.1:g.201328358C>A	GRCh37
NC_000001.9:g.199594981C>A	NCBI36
NG_007556.1:g.23448G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.862G>T	ENSP00000402238.3:p.Val288Phe
ENST00000367318.10:c.847G>T	ENSP00000356287.5:p.Val283Phe
ENST00000367322.6:c.835G>T	ENSP00000356291.2:p.Val279Phe
ENST00000412633.3:c.838G>T	ENSP00000408731.2:p.Val280Phe
ENST00000422165.6:c.868G>T	ENSP00000395163.2:p.Val290Phe
ENST00000438742.6:c.826G>T	ENSP00000414036.2:p.Val276Phe
ENST00000651504.1:n.1338G>T
ENST00000656932.1:c.877G>T MANE Select	ENSP00000499593.1:p.Val293Phe
ENST00000658476.1:c.912G>T	ENSP00000499741.1:p.Lys304Asn
ENST00000660295.1:c.847G>T	ENSP00000499418.1:p.Val283Phe
ENST00000662159.1:c.*236G>T	ENSP00000499796.1:n.*236G>T
ENST00000663843.1:c.*777G>T	ENSP00000499590.1:n.*777G>T
ENST00000666449.1:c.*122G>T	ENSP00000499667.1:n.*122G>T
ENST00000236918.11:c.877G>T	ENSP00000236918.8:p.Val293Phe
ENST00000360372.8:c.748G>T	ENSP00000353535.5:p.Val250Phe
ENST00000367315.6:c.856G>T	ENSP00000356284.3:p.Val286Phe
ENST00000367317.8:c.829G>T	ENSP00000356286.5:p.Val277Phe
ENST00000367318.9:c.847G>T	ENSP00000356287.5:p.Val283Phe
ENST00000367320.6:c.748G>T	ENSP00000356289.2:p.Val250Phe
ENST00000367322.5:c.838G>T	ENSP00000356291.1:p.Val280Phe
ENST00000421663.6:c.661G>T	ENSP00000404134.3:p.Val221Phe
ENST00000458432.6:c.661G>T	ENSP00000387874.3:p.Val221Phe
ENST00000460780.5:n.1996G>T
ENST00000476888.5:n.294G>T
ENST00000491504.5:n.2086G>T
ENST00000509001.5:c.847G>T	ENSP00000422031.1:p.Val283Phe
NM_000364.3:c.868G>T	NP_000355.2:p.Val290Phe
NM_001001430.2:c.847G>T	NP_001001430.1:p.Val283Phe
NM_001001431.2:c.838G>T	NP_001001431.1:p.Val280Phe
NM_001001432.2:c.829G>T	NP_001001432.1:p.Val277Phe
NM_001276345.1:c.877G>T	NP_001263274.1:p.Val293Phe
NM_001276346.1:c.748G>T	NP_001263275.1:p.Val250Phe
NM_001276347.1:c.847G>T	NP_001263276.1:p.Val283Phe
XM_006711508.2:c.847G>T	XP_006711571.1:p.Val283Phe
XM_006711509.2:c.844G>T	XP_006711572.1:p.Val282Phe
XM_011509938.1:c.877G>T	XP_011508240.1:p.Val293Phe
XM_011509939.1:c.874G>T	XP_011508241.1:p.Val292Phe
XM_011509940.1:c.874G>T	XP_011508242.1:p.Val292Phe
XM_011509941.1:c.871G>T	XP_011508243.1:p.Val291Phe
XM_011509942.1:c.832G>T	XP_011508244.1:p.Val278Phe
XM_011509943.1:c.832G>T	XP_011508245.1:p.Val278Phe
XM_011509944.1:c.829G>T	XP_011508246.1:p.Val277Phe
XM_011509946.1:c.670G>T	XP_011508248.1:p.Val224Phe
XM_006711508.3:c.847G>T	XP_006711571.1:p.Val283Phe
XM_006711509.3:c.844G>T	XP_006711572.1:p.Val282Phe
XM_011509938.2:c.877G>T	XP_011508240.1:p.Val293Phe
XM_011509940.2:c.874G>T	XP_011508242.1:p.Val292Phe
XM_011509941.2:c.871G>T	XP_011508243.1:p.Val291Phe
XM_011509942.2:c.832G>T	XP_011508244.1:p.Val278Phe
XM_011509943.2:c.832G>T	XP_011508245.1:p.Val278Phe
XM_011509944.2:c.829G>T	XP_011508246.1:p.Val277Phe
XM_017002216.2:c.844G>T	XP_016857705.1:p.Val282Phe
XM_017002217.1:c.838G>T	XP_016857706.1:p.Val280Phe
XM_024449450.1:c.877G>T	XP_024305218.1:p.Val293Phe
XM_024449454.1:c.844G>T	XP_024305222.1:p.Val282Phe
XM_024449455.1:c.844G>T	XP_024305223.1:p.Val282Phe
NM_000364.4:c.868G>T	NP_000355.2:p.Val290Phe
NM_001001430.3:c.847G>T	NP_001001430.1:p.Val283Phe
NM_001001431.3:c.838G>T	NP_001001431.1:p.Val280Phe
NM_001001432.3:c.829G>T	NP_001001432.1:p.Val277Phe
NM_001276345.2:c.877G>T MANE Select	NP_001263274.1:p.Val293Phe
NM_001276346.2:c.748G>T	NP_001263275.1:p.Val250Phe
NM_001276347.2:c.847G>T	NP_001263276.1:p.Val283Phe