Canonical Allele Identifier: CA2782277403
Gene: NDRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133248546_133248547insCCGCTTACCGCGAGTCTCACACAGGACCCGGGCTCT , CM000670.2:g.133248546_133248547insCCGCTTACCGCGAGTCTCACACAGGACCCGGGCTCT GRCh38
NC_000008.10:g.134260789_134260790insCCGCTTACCGCGAGTCTCACACAGGACCCGGGCTCT , CM000670.1:g.134260789_134260790insCCGCTTACCGCGAGTCTCACACAGGACCCGGGCTCT GRCh37
NC_000008.9:g.134329971_134329972insCCGCTTACCGCGAGTCTCACACAGGACCCGGGCTCT NCBI36
NG_007943.1:g.53709_53710insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG , LRG_258:g.53709_53710insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG MANE Select ENSP00000319977.8:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGAC...
ENST00000537882.3:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG ENSP00000437443.2:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGAC...
ENST00000675068.1:c.57+168_57+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG
ENST00000675860.1:n.520+168_520+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG
ENST00000323851.11:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG ENSP00000319977.7:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGAC...
ENST00000414097.6:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG ENSP00000404854.2:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGAC...
ENST00000517331.5:n.473+168_473+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG
ENST00000517599.5:c.*361+168_*361+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG ENSP00000429172.1:n.*361+168_*361+169insAGAGCCCGGGTCCTGTGTGAG...
ENST00000518066.5:c.37-6491_37-6490insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG ENSP00000431057.1:n.37-6491_37-6490insAGAGCCCGGGTCCTGTGTGAGAC...
ENST00000518176.5:c.49-1884_49-1883insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG ENSP00000429007.1:n.49-1884_49-1883insAGAGCCCGGGTCCTGTGTGAGAC...
ENST00000519278.5:n.1851+168_1851+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG
ENST00000521414.5:n.217+168_217+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG
ENST00000521664.1:n.505+168_505+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG
ENST00000522377.5:c.*235+168_*235+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG ENSP00000429380.1:n.*235+168_*235+169insAGAGCCCGGGTCCTGTGTGAG...
ENST00000522476.5:c.557+168_557+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG ENSP00000427894.1:n.557+168_557+169insAGAGCCCGGGTCCTGTGTGAGAC...
ENST00000522665.5:n.78+168_78+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG
ENST00000537882.2:c.512+168_512+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG ENSP00000437443.1:n.512+168_512+169insAGAGCCCGGGTCCTGTGTGAGAC...
NM_001135242.1:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001128714.1:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_001258432.1:c.557+168_557+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001245361.1:n.557+168_557+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_001258433.1:c.512+168_512+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001245362.1:n.512+168_512+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_006096.3:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG , LRG_258t1:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_006087.2:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGG...
XM_011516791.1:c.806+168_806+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG XP_011515093.1:n.806+168_806+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
XM_011516792.1:c.188+168_188+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG XP_011515094.1:n.188+168_188+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
XM_011516792.2:c.188+168_188+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG XP_011515094.1:n.188+168_188+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_001135242.2:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001128714.1:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_001258432.2:c.557+168_557+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001245361.1:n.557+168_557+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_001258433.2:c.512+168_512+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001245362.1:n.512+168_512+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_001374844.1:c.806+168_806+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001361773.1:n.806+168_806+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_001374845.1:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001361774.1:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_001374846.1:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001361775.1:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_001374847.1:c.557+168_557+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG NP_001361776.1:n.557+168_557+169insAGAGCCCGGGTCCTGTGTGAGACTCG...
NM_006096.4:c.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGGTAAGCGG MANE Select NP_006087.2:n.755+168_755+169insAGAGCCCGGGTCCTGTGTGAGACTCGCGG...