Canonical Allele Identifier: CA2688673871
Gene: NDRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133248693G>C , CM000670.2:g.133248693G>C GRCh38
NC_000008.10:g.134260936G>C , CM000670.1:g.134260936G>C GRCh37
NC_000008.9:g.134330118G>C NCBI36
NG_007943.1:g.53563C>G , LRG_258:g.53563C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323851.13:c.755+22C>G MANE Select ENSP00000319977.8:n.755+22C>G
ENST00000537882.3:c.755+22C>G ENSP00000437443.2:n.755+22C>G
ENST00000675068.1:c.57+22C>G
ENST00000675860.1:n.520+22C>G
ENST00000323851.11:c.755+22C>G ENSP00000319977.7:n.755+22C>G
ENST00000414097.6:c.755+22C>G ENSP00000404854.2:n.755+22C>G
ENST00000517331.5:n.473+22C>G
ENST00000517599.5:c.*361+22C>G ENSP00000429172.1:n.*361+22C>G
ENST00000518066.5:c.37-6637C>G ENSP00000431057.1:n.37-6637C>G
ENST00000518176.5:c.49-2030C>G ENSP00000429007.1:n.49-2030C>G
ENST00000519278.5:n.1851+22C>G
ENST00000521414.5:n.217+22C>G
ENST00000521664.1:n.505+22C>G
ENST00000522377.5:c.*235+22C>G ENSP00000429380.1:n.*235+22C>G
ENST00000522476.5:c.557+22C>G ENSP00000427894.1:n.557+22C>G
ENST00000522665.5:n.78+22C>G
ENST00000537882.2:c.512+22C>G ENSP00000437443.1:n.512+22C>G
NM_001135242.1:c.755+22C>G NP_001128714.1:n.755+22C>G
NM_001258432.1:c.557+22C>G NP_001245361.1:n.557+22C>G
NM_001258433.1:c.512+22C>G NP_001245362.1:n.512+22C>G
NM_006096.3:c.755+22C>G , LRG_258t1:c.755+22C>G NP_006087.2:n.755+22C>G
XM_011516791.1:c.806+22C>G XP_011515093.1:n.806+22C>G
XM_011516792.1:c.188+22C>G XP_011515094.1:n.188+22C>G
XM_011516792.2:c.188+22C>G XP_011515094.1:n.188+22C>G
NM_001135242.2:c.755+22C>G NP_001128714.1:n.755+22C>G
NM_001258432.2:c.557+22C>G NP_001245361.1:n.557+22C>G
NM_001258433.2:c.512+22C>G NP_001245362.1:n.512+22C>G
NM_001374844.1:c.806+22C>G NP_001361773.1:n.806+22C>G
NM_001374845.1:c.755+22C>G NP_001361774.1:n.755+22C>G
NM_001374846.1:c.755+22C>G NP_001361775.1:n.755+22C>G
NM_001374847.1:c.557+22C>G NP_001361776.1:n.557+22C>G
NM_006096.4:c.755+22C>G MANE Select NP_006087.2:n.755+22C>G