Canonical Allele Identifier: CA2688674221
Gene: NDRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133248875_133248878del , CM000670.2:g.133248875_133248878del GRCh38
NC_000008.10:g.134261118_134261121del , CM000670.1:g.134261118_134261121del GRCh37
NC_000008.9:g.134330300_134330303del NCBI36
NG_007943.1:g.53379_53382del , LRG_258:g.53379_53382del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.699-106_699-103del MANE Select ENSP00000319977.8:n.699-106_699-103del
ENST00000537882.3:c.699-106_699-103del ENSP00000437443.2:n.699-106_699-103del
ENST00000675056.1:n.29-106_29-103del
ENST00000675172.1:c.295-106_295-103del ENSP00000502297.1:n.295-106_295-103del
ENST00000675273.1:n.58-106_58-103del
ENST00000675860.1:n.464-106_464-103del
ENST00000676444.1:n.730-106_730-103del
ENST00000323851.11:c.699-106_699-103del ENSP00000319977.7:n.699-106_699-103del
ENST00000414097.6:c.699-106_699-103del ENSP00000404854.2:n.699-106_699-103del
ENST00000517331.5:n.417-106_417-103del
ENST00000517599.5:c.*305-106_*305-103del ENSP00000429172.1:n.*305-106_*305-103del
ENST00000518066.5:c.37-6821_37-6818del ENSP00000431057.1:n.37-6821_37-6818del
ENST00000518176.5:c.49-2214_49-2211del ENSP00000429007.1:n.49-2214_49-2211del
ENST00000519278.5:n.1795-106_1795-103del
ENST00000521414.5:n.161-106_161-103del
ENST00000521664.1:n.449-106_449-103del
ENST00000522377.5:c.*179-106_*179-103del ENSP00000429380.1:n.*179-106_*179-103del
ENST00000522476.5:c.501-106_501-103del ENSP00000427894.1:n.501-106_501-103del
ENST00000522665.5:n.22-106_22-103del
ENST00000537882.2:c.456-106_456-103del ENSP00000437443.1:n.456-106_456-103del
NM_001135242.1:c.699-106_699-103del NP_001128714.1:n.699-106_699-103del
NM_001258432.1:c.501-106_501-103del NP_001245361.1:n.501-106_501-103del
NM_001258433.1:c.456-106_456-103del NP_001245362.1:n.456-106_456-103del
NM_006096.3:c.699-106_699-103del , LRG_258t1:c.699-106_699-103del NP_006087.2:n.699-106_699-103del
XM_011516791.1:c.750-106_750-103del XP_011515093.1:n.750-106_750-103del
XM_011516792.1:c.132-106_132-103del XP_011515094.1:n.132-106_132-103del
XM_011516792.2:c.132-106_132-103del XP_011515094.1:n.132-106_132-103del
NM_001135242.2:c.699-106_699-103del NP_001128714.1:n.699-106_699-103del
NM_001258432.2:c.501-106_501-103del NP_001245361.1:n.501-106_501-103del
NM_001258433.2:c.456-106_456-103del NP_001245362.1:n.456-106_456-103del
NM_001374844.1:c.750-106_750-103del NP_001361773.1:n.750-106_750-103del
NM_001374845.1:c.699-106_699-103del NP_001361774.1:n.699-106_699-103del
NM_001374846.1:c.699-106_699-103del NP_001361775.1:n.699-106_699-103del
NM_001374847.1:c.501-106_501-103del NP_001361776.1:n.501-106_501-103del
NM_006096.4:c.699-106_699-103del MANE Select NP_006087.2:n.699-106_699-103del