Canonical Allele Identifier: CA1821166941
Gene: NDRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133249086_133249087delinsCT , CM000670.2:g.133249086_133249087delinsCT GRCh38
NC_000008.10:g.134261329_134261330delinsCT , CM000670.1:g.134261329_134261330delinsCT GRCh37
NC_000008.9:g.134330511_134330512delinsCT NCBI36
NG_007943.1:g.53169_53170delinsAG , LRG_258:g.53169_53170delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.699-316_699-315delinsAG MANE Select ENSP00000319977.8:n.699-316_699-315delinsAG
ENST00000537882.3:c.699-316_699-315delinsAG ENSP00000437443.2:n.699-316_699-315delinsAG
ENST00000675056.1:n.28+293_28+294delinsAG
ENST00000675172.1:c.295-316_295-315delinsAG ENSP00000502297.1:n.295-316_295-315delinsAG
ENST00000675273.1:n.58-316_58-315delinsAG
ENST00000675860.1:n.464-316_464-315delinsAG
ENST00000676444.1:n.730-316_730-315delinsAG
ENST00000323851.11:c.699-316_699-315delinsAG ENSP00000319977.7:n.699-316_699-315delinsAG
ENST00000414097.6:c.699-316_699-315delinsAG ENSP00000404854.2:n.699-316_699-315delinsAG
ENST00000517331.5:n.417-316_417-315delinsAG
ENST00000517599.5:c.*305-316_*305-315delinsAG ENSP00000429172.1:n.*305-316_*305-315delinsAG
ENST00000518066.5:c.37-7031_37-7030delinsAG ENSP00000431057.1:n.37-7031_37-7030delinsAG
ENST00000518176.5:c.49-2424_49-2423delinsAG ENSP00000429007.1:n.49-2424_49-2423delinsAG
ENST00000519278.5:n.1795-316_1795-315delinsAG
ENST00000521414.5:n.160+242_160+243delinsAG
ENST00000521664.1:n.449-316_449-315delinsAG
ENST00000522377.5:c.*179-316_*179-315delinsAG ENSP00000429380.1:n.*179-316_*179-315delinsAG
ENST00000522476.5:c.501-316_501-315delinsAG ENSP00000427894.1:n.501-316_501-315delinsAG
ENST00000522665.5:n.22-316_22-315delinsAG
ENST00000537882.2:c.456-316_456-315delinsAG ENSP00000437443.1:n.456-316_456-315delinsAG
NM_001135242.1:c.699-316_699-315delinsAG NP_001128714.1:n.699-316_699-315delinsAG
NM_001258432.1:c.501-316_501-315delinsAG NP_001245361.1:n.501-316_501-315delinsAG
NM_001258433.1:c.456-316_456-315delinsAG NP_001245362.1:n.456-316_456-315delinsAG
NM_006096.3:c.699-316_699-315delinsAG , LRG_258t1:c.699-316_699-315delinsAG NP_006087.2:n.699-316_699-315delinsAG
XM_011516791.1:c.750-316_750-315delinsAG XP_011515093.1:n.750-316_750-315delinsAG
XM_011516792.1:c.132-316_132-315delinsAG XP_011515094.1:n.132-316_132-315delinsAG
XM_011516792.2:c.132-316_132-315delinsAG XP_011515094.1:n.132-316_132-315delinsAG
NM_001135242.2:c.699-316_699-315delinsAG NP_001128714.1:n.699-316_699-315delinsAG
NM_001258432.2:c.501-316_501-315delinsAG NP_001245361.1:n.501-316_501-315delinsAG
NM_001258433.2:c.456-316_456-315delinsAG NP_001245362.1:n.456-316_456-315delinsAG
NM_001374844.1:c.750-316_750-315delinsAG NP_001361773.1:n.750-316_750-315delinsAG
NM_001374845.1:c.699-316_699-315delinsAG NP_001361774.1:n.699-316_699-315delinsAG
NM_001374846.1:c.699-316_699-315delinsAG NP_001361775.1:n.699-316_699-315delinsAG
NM_001374847.1:c.501-316_501-315delinsAG NP_001361776.1:n.501-316_501-315delinsAG
NM_006096.4:c.699-316_699-315delinsAG MANE Select NP_006087.2:n.699-316_699-315delinsAG