Canonical Allele Identifier: CA344204237
Gene: TNNT2 HGNC NCBI

Linked Data

dbSNP Id: rs1376311899

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201363296C>A , CM000663.2:g.201363296C>A GRCh38
NC_000001.10:g.201332424C>A , CM000663.1:g.201332424C>A GRCh37
NC_000001.9:g.199599047C>A NCBI36
NG_007556.1:g.19382G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000455702.7:c.585G>T ENSP00000402238.3:p.Lys195Asn
ENST00000367318.10:c.570G>T ENSP00000356287.5:p.Lys190Asn
ENST00000367322.6:c.567G>T ENSP00000356291.2:p.Lys189Asn
ENST00000412633.3:c.570G>T ENSP00000408731.2:p.Lys190Asn
ENST00000422165.6:c.600G>T ENSP00000395163.2:p.Lys200Asn
ENST00000438742.6:c.552G>T ENSP00000414036.2:p.Lys184Asn
ENST00000455702.6:c.585G>T ENSP00000402238.2:p.Lys195Asn
ENST00000651504.1:n.1064G>T
ENST00000656932.1:c.600G>T MANE Select ENSP00000499593.1:p.Lys200Asn
ENST00000658476.1:c.570G>T ENSP00000499741.1:p.Lys190Asn
ENST00000660295.1:c.570G>T ENSP00000499418.1:p.Lys190Asn
ENST00000662159.1:c.163-1297G>T ENSP00000499796.1:n.163-1297G>T
ENST00000663843.1:c.*500G>T ENSP00000499590.1:n.*500G>T
ENST00000666449.1:c.570G>T ENSP00000499667.1:p.Lys190Asn
ENST00000236918.11:c.600G>T ENSP00000236918.8:p.Lys200Asn
ENST00000360372.8:c.480G>T ENSP00000353535.5:p.Lys160Asn
ENST00000367315.6:c.576G>T ENSP00000356284.3:p.Lys192Asn
ENST00000367317.8:c.555G>T ENSP00000356286.5:p.Lys185Asn
ENST00000367318.9:c.570G>T ENSP00000356287.5:p.Lys190Asn
ENST00000367320.6:c.480G>T ENSP00000356289.2:p.Lys160Asn
ENST00000367322.5:c.570G>T ENSP00000356291.1:p.Lys190Asn
ENST00000421663.6:c.393G>T ENSP00000404134.3:p.Lys131Asn
ENST00000438742.5:c.555G>T ENSP00000414036.1:p.Lys185Asn
ENST00000458432.6:c.393G>T ENSP00000387874.3:p.Lys131Asn
ENST00000460780.5:n.893G>T
ENST00000476888.5:n.55G>T
ENST00000491504.5:n.1809G>T
ENST00000509001.5:c.570G>T ENSP00000422031.1:p.Lys190Asn
ENST00000515042.5:n.496G>T
NM_000364.3:c.600G>T NP_000355.2:p.Lys200Asn
NM_001001430.2:c.570G>T NP_001001430.1:p.Lys190Asn
NM_001001431.2:c.570G>T NP_001001431.1:p.Lys190Asn
NM_001001432.2:c.555G>T NP_001001432.1:p.Lys185Asn
NM_001276345.1:c.600G>T NP_001263274.1:p.Lys200Asn
NM_001276346.1:c.480G>T NP_001263275.1:p.Lys160Asn
NM_001276347.1:c.570G>T NP_001263276.1:p.Lys190Asn
XM_006711508.2:c.570G>T XP_006711571.1:p.Lys190Asn
XM_006711509.2:c.567G>T XP_006711572.1:p.Lys189Asn
XM_011509938.1:c.600G>T XP_011508240.1:p.Lys200Asn
XM_011509939.1:c.597G>T XP_011508241.1:p.Lys199Asn
XM_011509940.1:c.600G>T XP_011508242.1:p.Lys200Asn
XM_011509941.1:c.597G>T XP_011508243.1:p.Lys199Asn
XM_011509942.1:c.555G>T XP_011508244.1:p.Lys185Asn
XM_011509943.1:c.555G>T XP_011508245.1:p.Lys185Asn
XM_011509944.1:c.552G>T XP_011508246.1:p.Lys184Asn
XM_011509946.1:c.393G>T XP_011508248.1:p.Lys131Asn
XM_006711508.3:c.570G>T XP_006711571.1:p.Lys190Asn
XM_006711509.3:c.567G>T XP_006711572.1:p.Lys189Asn
XM_011509938.2:c.600G>T XP_011508240.1:p.Lys200Asn
XM_011509940.2:c.600G>T XP_011508242.1:p.Lys200Asn
XM_011509941.2:c.597G>T XP_011508243.1:p.Lys199Asn
XM_011509942.2:c.555G>T XP_011508244.1:p.Lys185Asn
XM_011509943.2:c.555G>T XP_011508245.1:p.Lys185Asn
XM_011509944.2:c.552G>T XP_011508246.1:p.Lys184Asn
XM_017002216.2:c.570G>T XP_016857705.1:p.Lys190Asn
XM_017002217.1:c.570G>T XP_016857706.1:p.Lys190Asn
XM_024449450.1:c.600G>T XP_024305218.1:p.Lys200Asn
XM_024449454.1:c.567G>T XP_024305222.1:p.Lys189Asn
XM_024449455.1:c.570G>T XP_024305223.1:p.Lys190Asn
NM_000364.4:c.600G>T NP_000355.2:p.Lys200Asn
NM_001001430.3:c.570G>T NP_001001430.1:p.Lys190Asn
NM_001001431.3:c.570G>T NP_001001431.1:p.Lys190Asn
NM_001001432.3:c.555G>T NP_001001432.1:p.Lys185Asn
NM_001276345.2:c.600G>T MANE Select NP_001263274.1:p.Lys200Asn
NM_001276346.2:c.480G>T NP_001263275.1:p.Lys160Asn
NM_001276347.2:c.570G>T NP_001263276.1:p.Lys190Asn