Canonical Allele Identifier: CA10576370
Community Standard Title: NM_001276345.2(TNNT2):c.854C>A (p.Ser285Tyr)
Gene: TNNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201359253G>T , CM000663.2:g.201359253G>T GRCh38
NC_000001.10:g.201328381G>T , CM000663.1:g.201328381G>T GRCh37
NC_000001.9:g.199595004G>T NCBI36
NG_007556.1:g.23425C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001276345.2:c.854C>A MANE Select NP_001263274.1:p.Ser285Tyr
ENST00000656932.1:c.854C>A MANE Select ENSP00000499593.1:p.Ser285Tyr
NM_000364.3:c.845C>A NP_000355.2:p.Ser282Tyr
NM_000364.4:c.845C>A NP_000355.2:p.Ser282Tyr
NM_001001430.2:c.824C>A NP_001001430.1:p.Ser275Tyr
NM_001001430.3:c.824C>A NP_001001430.1:p.Ser275Tyr
NM_001001431.2:c.815C>A NP_001001431.1:p.Ser272Tyr
NM_001001431.3:c.815C>A NP_001001431.1:p.Ser272Tyr
NM_001001432.2:c.806C>A NP_001001432.1:p.Ser269Tyr
NM_001001432.3:c.806C>A NP_001001432.1:p.Ser269Tyr
NM_001276345.1:c.854C>A NP_001263274.1:p.Ser285Tyr
NM_001276346.1:c.725C>A NP_001263275.1:p.Ser242Tyr
NM_001276346.2:c.725C>A NP_001263275.1:p.Ser242Tyr
NM_001276347.1:c.824C>A NP_001263276.1:p.Ser275Tyr
NM_001276347.2:c.824C>A NP_001263276.1:p.Ser275Tyr
ENST00000236918.11:c.854C>A ENSP00000236918.8:p.Ser285Tyr
ENST00000360372.8:c.725C>A ENSP00000353535.5:p.Ser242Tyr
ENST00000367315.6:c.833C>A ENSP00000356284.3:p.Ser278Tyr
ENST00000367317.8:c.806C>A ENSP00000356286.5:p.Ser269Tyr
ENST00000367318.10:c.824C>A ENSP00000356287.5:p.Ser275Tyr
ENST00000367318.9:c.824C>A ENSP00000356287.5:p.Ser275Tyr
ENST00000367320.6:c.725C>A ENSP00000356289.2:p.Ser242Tyr
ENST00000367322.5:c.815C>A ENSP00000356291.1:p.Ser272Tyr
ENST00000367322.6:c.812C>A ENSP00000356291.2:p.Ser271Tyr
ENST00000412633.3:c.815C>A ENSP00000408731.2:p.Ser272Tyr
ENST00000421663.6:c.638C>A ENSP00000404134.3:p.Ser213Tyr
ENST00000422165.6:c.845C>A ENSP00000395163.2:p.Ser282Tyr
ENST00000438742.5:c.806C>A ENSP00000414036.1:p.Ser269Tyr
ENST00000438742.6:c.803C>A ENSP00000414036.2:p.Ser268Tyr
ENST00000455702.7:c.839C>A ENSP00000402238.3:p.Ser280Tyr
ENST00000458432.6:c.638C>A ENSP00000387874.3:p.Ser213Tyr
ENST00000460780.5:n.1973C>A
ENST00000476888.5:n.271C>A
ENST00000491504.5:n.2063C>A
ENST00000509001.5:c.824C>A ENSP00000422031.1:p.Ser275Tyr
ENST00000651504.1:n.1315C>A
ENST00000658476.1:c.889C>A ENSP00000499741.1:p.Pro297Thr
ENST00000660295.1:c.824C>A ENSP00000499418.1:p.Ser275Tyr
ENST00000662159.1:c.*213C>A ENSP00000499796.1:n.*213C>A
ENST00000663843.1:c.*754C>A ENSP00000499590.1:n.*754C>A
ENST00000666449.1:c.*99C>A ENSP00000499667.1:n.*99C>A
XM_006711508.2:c.824C>A XP_006711571.1:p.Ser275Tyr
XM_006711508.3:c.824C>A XP_006711571.1:p.Ser275Tyr
XM_006711509.2:c.821C>A XP_006711572.1:p.Ser274Tyr
XM_006711509.3:c.821C>A XP_006711572.1:p.Ser274Tyr
XM_011509938.1:c.854C>A XP_011508240.1:p.Ser285Tyr
XM_011509938.2:c.854C>A XP_011508240.1:p.Ser285Tyr
XM_011509939.1:c.851C>A XP_011508241.1:p.Ser284Tyr
XM_011509940.1:c.851C>A XP_011508242.1:p.Ser284Tyr
XM_011509940.2:c.851C>A XP_011508242.1:p.Ser284Tyr
XM_011509941.1:c.848C>A XP_011508243.1:p.Ser283Tyr
XM_011509941.2:c.848C>A XP_011508243.1:p.Ser283Tyr
XM_011509942.1:c.809C>A XP_011508244.1:p.Ser270Tyr
XM_011509942.2:c.809C>A XP_011508244.1:p.Ser270Tyr
XM_011509943.1:c.809C>A XP_011508245.1:p.Ser270Tyr
XM_011509943.2:c.809C>A XP_011508245.1:p.Ser270Tyr
XM_011509944.1:c.806C>A XP_011508246.1:p.Ser269Tyr
XM_011509944.2:c.806C>A XP_011508246.1:p.Ser269Tyr
XM_011509946.1:c.647C>A XP_011508248.1:p.Ser216Tyr
XM_017002216.2:c.821C>A XP_016857705.1:p.Ser274Tyr
XM_017002217.1:c.815C>A XP_016857706.1:p.Ser272Tyr
XM_024449450.1:c.854C>A XP_024305218.1:p.Ser285Tyr
XM_024449454.1:c.821C>A XP_024305222.1:p.Ser274Tyr
XM_024449455.1:c.821C>A XP_024305223.1:p.Ser274Tyr