LDH info

Canonical Allele Identifier: CA16615727
Gene: TP53 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 406611
ClinVar RCV Id: RCV000464864
dbSNP Id: rs1060501212

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7674973_7674975del , CM000679.2:g.7674973_7674975del GRCh38
NC_000017.10:g.7578291_7578293del , CM000679.1:g.7578291_7578293del GRCh37
NC_000017.9:g.7519016_7519018del NCBI36
NG_017013.2:g.17576_17578del , LRG_321:g.17576_17578del

Transcript Alleles

HGVS Amino-acid change
NM_000546.5:c.560-4_560-2del , LRG_321t1:c.560-4_560-2del NP_000537.3:p.=
NM_001126112.2:c.560-4_560-2del , LRG_321t2:c.560-4_560-2del NP_001119584.1:p.=
NM_001126113.2:c.560-4_560-2del , LRG_321t4:c.560-4_560-2del NP_001119585.1:p.=
NM_001126114.2:c.560-4_560-2del , LRG_321t3:c.560-4_560-2del NP_001119586.1:p.=
NM_001126115.1:c.164-4_164-2del , LRG_321t5:c.164-4_164-2del NP_001119587.1:p.=
NM_001126116.1:c.164-4_164-2del , LRG_321t6:c.164-4_164-2del NP_001119588.1:p.=
NM_001126117.1:c.164-4_164-2del , LRG_321t7:c.164-4_164-2del NP_001119589.1:p.=
NM_001126118.1:c.443-4_443-2del , LRG_321t8:c.443-4_443-2del NP_001119590.1:p.=
NM_001276695.1:c.443-4_443-2del VV NP_001263624.1:p.=
NM_001276696.1:c.443-4_443-2del VV NP_001263625.1:p.=
NM_001276697.1:c.83-4_83-2del VV NP_001263626.1:p.=
NM_001276698.1:c.83-4_83-2del VV NP_001263627.1:p.=
NM_001276699.1:c.83-4_83-2del VV NP_001263628.1:p.=
NM_001276760.1:c.443-4_443-2del VV NP_001263689.1:p.=
NM_001276761.1:c.443-4_443-2del VV NP_001263690.1:p.=
NM_001276695.2:c.443-4_443-2del VV NP_001263624.1:p.=
NM_001276696.2:c.443-4_443-2del VV NP_001263625.1:p.=
NM_001276697.2:c.83-4_83-2del VV NP_001263626.1:p.=
NM_001276698.2:c.83-4_83-2del VV NP_001263627.1:p.=
NM_001276699.2:c.83-4_83-2del VV NP_001263628.1:p.=
NM_001276760.2:c.443-4_443-2del VV NP_001263689.1:p.=
NM_001276761.2:c.443-4_443-2del VV NP_001263690.1:p.=
ENST00000269305.8:c.560-4_560-2del ENSP00000269305.4:p.=
ENST00000359597.8:n.560-4_560-2del ENSP00000352610.4:p.=
ENST00000413465.6:n.560-4_560-2del ENSP00000410739.2:p.=
ENST00000420246.6:c.560-4_560-2del ENSP00000391127.2:p.=
ENST00000445888.6:c.560-4_560-2del ENSP00000391478.2:p.=
ENST00000455263.6:c.560-4_560-2del ENSP00000398846.2:p.=
ENST00000504290.5:c.164-4_164-2del ENSP00000484409.1:p.=
ENST00000504937.5:c.164-4_164-2del ENSP00000481179.1:p.=
ENST00000505014.5:n.816-4_816-2del
ENST00000509690.5:c.164-4_164-2del ENSP00000425104.1:p.=
ENST00000510385.5:c.164-4_164-2del ENSP00000478499.1:p.=
ENST00000514944.5:c.281-4_281-2del ENSP00000423862.1:p.=
ENST00000574684.1:n.67+78_67+80del
ENST00000610292.4:c.443-4_443-2del ENSP00000478219.1:p.=
ENST00000610538.4:c.443-4_443-2del ENSP00000480868.1:p.=
ENST00000610623.4:c.83-4_83-2del ENSP00000477531.1:p.=
ENST00000615910.4:n.527-4_527-2del ENSP00000482903.1:p.=
ENST00000617185.4:c.560-4_560-2del ENSP00000482258.1:p.=
ENST00000618944.4:c.83-4_83-2del ENSP00000481401.1:p.=
ENST00000619186.4:c.83-4_83-2del ENSP00000484375.1:p.=
ENST00000619485.4:c.443-4_443-2del ENSP00000482537.1:p.=
ENST00000620739.4:c.443-4_443-2del ENSP00000481638.1:p.=
ENST00000622645.4:c.443-4_443-2del ENSP00000482222.1:p.=
ENST00000635293.1:c.443-4_443-2del ENSP00000488924.1:p.=