Canonical Allele Identifier: CA344201881

Gene: TNNT2

Linked Data

• MyVariant Identifiers: chr1:g.201328366T>A (hg19) ; chr1:g.201359238T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359238T>A , CM000663.2:g.201359238T>A	GRCh38
NC_000001.10:g.201328366T>A , CM000663.1:g.201328366T>A	GRCh37
NC_000001.9:g.199594989T>A	NCBI36
NG_007556.1:g.23440A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.854A>T	ENSP00000402238.3:p.Lys285Met
ENST00000367318.10:c.839A>T	ENSP00000356287.5:p.Lys280Met
ENST00000367322.6:c.827A>T	ENSP00000356291.2:p.Lys276Met
ENST00000412633.3:c.830A>T	ENSP00000408731.2:p.Lys277Met
ENST00000422165.6:c.860A>T	ENSP00000395163.2:p.Lys287Met
ENST00000438742.6:c.818A>T	ENSP00000414036.2:p.Lys273Met
ENST00000651504.1:n.1330A>T
ENST00000656932.1:c.869A>T MANE Select	ENSP00000499593.1:p.Lys290Met
ENST00000658476.1:c.904A>T	ENSP00000499741.1:p.Arg302Trp
ENST00000660295.1:c.839A>T	ENSP00000499418.1:p.Lys280Met
ENST00000662159.1:c.*228A>T	ENSP00000499796.1:n.*228A>T
ENST00000663843.1:c.*769A>T	ENSP00000499590.1:n.*769A>T
ENST00000666449.1:c.*114A>T	ENSP00000499667.1:n.*114A>T
ENST00000236918.11:c.869A>T	ENSP00000236918.8:p.Lys290Met
ENST00000360372.8:c.740A>T	ENSP00000353535.5:p.Lys247Met
ENST00000367315.6:c.848A>T	ENSP00000356284.3:p.Lys283Met
ENST00000367317.8:c.821A>T	ENSP00000356286.5:p.Lys274Met
ENST00000367318.9:c.839A>T	ENSP00000356287.5:p.Lys280Met
ENST00000367320.6:c.740A>T	ENSP00000356289.2:p.Lys247Met
ENST00000367322.5:c.830A>T	ENSP00000356291.1:p.Lys277Met
ENST00000421663.6:c.653A>T	ENSP00000404134.3:p.Lys218Met
ENST00000458432.6:c.653A>T	ENSP00000387874.3:p.Lys218Met
ENST00000460780.5:n.1988A>T
ENST00000476888.5:n.286A>T
ENST00000491504.5:n.2078A>T
ENST00000509001.5:c.839A>T	ENSP00000422031.1:p.Lys280Met
NM_000364.3:c.860A>T	NP_000355.2:p.Lys287Met
NM_001001430.2:c.839A>T	NP_001001430.1:p.Lys280Met
NM_001001431.2:c.830A>T	NP_001001431.1:p.Lys277Met
NM_001001432.2:c.821A>T	NP_001001432.1:p.Lys274Met
NM_001276345.1:c.869A>T	NP_001263274.1:p.Lys290Met
NM_001276346.1:c.740A>T	NP_001263275.1:p.Lys247Met
NM_001276347.1:c.839A>T	NP_001263276.1:p.Lys280Met
XM_006711508.2:c.839A>T	XP_006711571.1:p.Lys280Met
XM_006711509.2:c.836A>T	XP_006711572.1:p.Lys279Met
XM_011509938.1:c.869A>T	XP_011508240.1:p.Lys290Met
XM_011509939.1:c.866A>T	XP_011508241.1:p.Lys289Met
XM_011509940.1:c.866A>T	XP_011508242.1:p.Lys289Met
XM_011509941.1:c.863A>T	XP_011508243.1:p.Lys288Met
XM_011509942.1:c.824A>T	XP_011508244.1:p.Lys275Met
XM_011509943.1:c.824A>T	XP_011508245.1:p.Lys275Met
XM_011509944.1:c.821A>T	XP_011508246.1:p.Lys274Met
XM_011509946.1:c.662A>T	XP_011508248.1:p.Lys221Met
XM_006711508.3:c.839A>T	XP_006711571.1:p.Lys280Met
XM_006711509.3:c.836A>T	XP_006711572.1:p.Lys279Met
XM_011509938.2:c.869A>T	XP_011508240.1:p.Lys290Met
XM_011509940.2:c.866A>T	XP_011508242.1:p.Lys289Met
XM_011509941.2:c.863A>T	XP_011508243.1:p.Lys288Met
XM_011509942.2:c.824A>T	XP_011508244.1:p.Lys275Met
XM_011509943.2:c.824A>T	XP_011508245.1:p.Lys275Met
XM_011509944.2:c.821A>T	XP_011508246.1:p.Lys274Met
XM_017002216.2:c.836A>T	XP_016857705.1:p.Lys279Met
XM_017002217.1:c.830A>T	XP_016857706.1:p.Lys277Met
XM_024449450.1:c.869A>T	XP_024305218.1:p.Lys290Met
XM_024449454.1:c.836A>T	XP_024305222.1:p.Lys279Met
XM_024449455.1:c.836A>T	XP_024305223.1:p.Lys279Met
NM_000364.4:c.860A>T	NP_000355.2:p.Lys287Met
NM_001001430.3:c.839A>T	NP_001001430.1:p.Lys280Met
NM_001001431.3:c.830A>T	NP_001001431.1:p.Lys277Met
NM_001001432.3:c.821A>T	NP_001001432.1:p.Lys274Met
NM_001276345.2:c.869A>T MANE Select	NP_001263274.1:p.Lys290Met
NM_001276346.2:c.740A>T	NP_001263275.1:p.Lys247Met
NM_001276347.2:c.839A>T	NP_001263276.1:p.Lys280Met