Canonical Allele Identifier: CA005245
Gene: TNNT2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12411
dbSNP Id: rs121964857

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201359245G>A , CM000663.2:g.201359245G>A GRCh38
NC_000001.10:g.201328373G>A , CM000663.1:g.201328373G>A GRCh37
NC_000001.9:g.199594996G>A NCBI36
NG_007556.1:g.23433C>T

Transcript Alleles

HGVS Amino-acid change
NM_000364.3:c.853C>T VV NP_000355.2:p.Arg285Cys
NM_001001430.2:c.832C>T VV NP_001001430.1:p.Arg278Cys
NM_001001431.2:c.823C>T VV NP_001001431.1:p.Arg275Cys
NM_001001432.2:c.814C>T VV NP_001001432.1:p.Arg272Cys
NM_001276345.1:c.862C>T VV NP_001263274.1:p.Arg288Cys
NM_001276346.1:c.733C>T VV NP_001263275.1:p.Arg245Cys
NM_001276347.1:c.832C>T VV NP_001263276.1:p.Arg278Cys
XM_006711508.2:c.832C>T XP_006711571.1:p.Arg278Cys
XM_006711509.2:c.829C>T XP_006711572.1:p.Arg277Cys
XM_011509938.1:c.862C>T XP_011508240.1:p.Arg288Cys
XM_011509939.1:c.859C>T XP_011508241.1:p.Arg287Cys
XM_011509940.1:c.859C>T XP_011508242.1:p.Arg287Cys
XM_011509941.1:c.856C>T XP_011508243.1:p.Arg286Cys
XM_011509942.1:c.817C>T XP_011508244.1:p.Arg273Cys
XM_011509943.1:c.817C>T XP_011508245.1:p.Arg273Cys
XM_011509944.1:c.814C>T XP_011508246.1:p.Arg272Cys
XM_011509946.1:c.655C>T XP_011508248.1:p.Arg219Cys
XM_006711508.3:c.832C>T
XM_006711509.3:c.829C>T
XM_011509938.2:c.862C>T
XM_011509940.2:c.859C>T
XM_011509941.2:c.856C>T
XM_011509942.2:c.817C>T
XM_011509943.2:c.817C>T
XM_011509944.2:c.814C>T
XM_017002216.2:c.829C>T XP_016857705.1:p.Arg277Cys
XM_017002217.1:c.823C>T XP_016857706.1:p.Arg275Cys
XM_024449450.1:c.862C>T XP_024305218.1:p.Arg288Cys
XM_024449454.1:c.829C>T XP_024305222.1:p.Arg277Cys
XM_024449455.1:c.829C>T XP_024305223.1:p.Arg277Cys
ENST00000236918.11:n.862C>T ENSP00000236918.8:p.Arg288Cys
ENST00000360372.8:n.733C>T ENSP00000353535.5:p.Arg245Cys
ENST00000367315.6:c.841C>T ENSP00000356284.3:p.Arg281Cys
ENST00000367317.8:n.814C>T ENSP00000356286.5:p.Arg272Cys
ENST00000367318.9:c.832C>T ENSP00000356287.5:p.Arg278Cys
ENST00000367320.6:c.733C>T ENSP00000356289.2:p.Arg245Cys
ENST00000367322.5:c.823C>T ENSP00000356291.1:p.Arg275Cys
ENST00000421663.6:c.646C>T ENSP00000404134.3:p.Arg216Cys
ENST00000438742.5:c.814C>T
ENST00000458432.6:c.646C>T ENSP00000387874.3:p.Arg216Cys
ENST00000460780.5:n.1981C>T
ENST00000476888.5:n.279C>T
ENST00000491504.5:n.2071C>T
ENST00000509001.5:c.832C>T ENSP00000422031.1:p.Arg278Cys