LDH info

Canonical Allele Identifier: CA004651
Gene: TNNT2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 43648
dbSNP Id: rs397516470

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201363386_201363388del , CM000663.2:g.201363386_201363388del GRCh38
NC_000001.10:g.201332514_201332516del , CM000663.1:g.201332514_201332516del GRCh37
NC_000001.9:g.199599137_199599139del NCBI36
NG_007556.1:g.19299_19301del

Transcript Alleles

HGVS Amino-acid change
NM_000364.3:c.517_519del VV NP_000355.2:p.Glu173del
NM_001001430.2:c.487_489del VV NP_001001430.1:p.Glu163del
NM_001001431.2:c.487_489del VV NP_001001431.1:p.Glu163del
NM_001001432.2:c.472_474del VV NP_001001432.1:p.Glu158del
NM_001276345.1:c.517_519del VV NP_001263274.1:p.Glu173del
NM_001276346.1:c.397_399del VV NP_001263275.1:p.Glu133del
NM_001276347.1:c.487_489del VV NP_001263276.1:p.Glu163del
XM_006711508.2:c.487_489del XP_006711571.1:p.Glu163del
XM_006711509.2:c.484_486del XP_006711572.1:p.Glu162del
XM_011509938.1:c.517_519del XP_011508240.1:p.Glu173del
XM_011509939.1:c.514_516del XP_011508241.1:p.Glu172del
XM_011509940.1:c.517_519del XP_011508242.1:p.Glu173del
XM_011509941.1:c.514_516del XP_011508243.1:p.Glu172del
XM_011509942.1:c.472_474del XP_011508244.1:p.Glu158del
XM_011509943.1:c.472_474del XP_011508245.1:p.Glu158del
XM_011509944.1:c.469_471del XP_011508246.1:p.Glu157del
XM_011509946.1:c.310_312del XP_011508248.1:p.Glu104del
XM_006711508.3:c.487_489del XP_006711571.1:p.Glu163del
XM_006711509.3:c.484_486del XP_006711572.1:p.Glu162del
XM_011509938.2:c.517_519del XP_011508240.1:p.Glu173del
XM_011509940.2:c.517_519del XP_011508242.1:p.Glu173del
XM_011509941.2:c.514_516del XP_011508243.1:p.Glu172del
XM_011509942.2:c.472_474del XP_011508244.1:p.Glu158del
XM_011509943.2:c.472_474del XP_011508245.1:p.Glu158del
XM_011509944.2:c.469_471del XP_011508246.1:p.Glu157del
XM_017002216.2:c.487_489del XP_016857705.1:p.Glu163del
XM_017002217.1:c.487_489del XP_016857706.1:p.Glu163del
XM_024449450.1:c.517_519del XP_024305218.1:p.Glu173del
XM_024449454.1:c.484_486del XP_024305222.1:p.Glu162del
XM_024449455.1:c.487_489del XP_024305223.1:p.Glu163del
NM_000364.4:c.517_519del VV NP_000355.2:p.Glu173del
NM_001001430.3:c.487_489del VV NP_001001430.1:p.Glu163del
NM_001001431.3:c.487_489del VV NP_001001431.1:p.Glu163del
NM_001001432.3:c.472_474del VV NP_001001432.1:p.Glu158del
NM_001276345.2:c.517_519del VV NP_001263274.1:p.Glu173del
NM_001276346.2:c.397_399del VV NP_001263275.1:p.Glu133del
NM_001276347.2:c.487_489del VV NP_001263276.1:p.Glu163del
ENST00000236918.11:n.517_519del ENSP00000236918.8:p.Glu173del
ENST00000360372.8:n.397_399del ENSP00000353535.5:p.Glu133del
ENST00000367315.6:c.493_495del ENSP00000356284.3:p.Glu165del
ENST00000367317.8:n.472_474del ENSP00000356286.5:p.Glu158del
ENST00000367318.9:c.487_489del ENSP00000356287.5:p.Glu163del
ENST00000367320.6:c.397_399del ENSP00000356289.2:p.Glu133del
ENST00000367322.5:c.487_489del ENSP00000356291.1:p.Glu163del
ENST00000421663.6:c.310_312del ENSP00000404134.3:p.Glu104del
ENST00000438742.5:c.472_474del ENSP00000414036.1:p.Glu158del
ENST00000455702.5:c.517_519del ENSP00000402238.1:p.Glu173del
ENST00000458432.6:c.310_312del ENSP00000387874.3:p.Glu104del
ENST00000460780.5:n.810_812del
ENST00000466570.5:n.743_745del
ENST00000491504.5:n.1726_1728del
ENST00000509001.5:c.487_489del ENSP00000422031.1:p.Glu163del
ENST00000515042.5:n.413_415del