Canonical Allele Identifier: CA1821166989
Gene: NDRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133249145G= , CM000670.2:g.133249145G= GRCh38
NC_000008.10:g.134261388G= , CM000670.1:g.134261388G= GRCh37
NC_000008.9:g.134330570G= NCBI36
NG_007943.1:g.53111C= , LRG_258:g.53111C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.699-374C= MANE Select ENSP00000319977.8:n.699-374C=
ENST00000537882.3:c.699-374C= ENSP00000437443.2:n.699-374C=
ENST00000675056.1:n.28+235C=
ENST00000675172.1:c.295-374C= ENSP00000502297.1:n.295-374C=
ENST00000675273.1:n.58-374C=
ENST00000675860.1:n.464-374C=
ENST00000676444.1:n.730-374C=
ENST00000323851.11:c.699-374C= ENSP00000319977.7:n.699-374C=
ENST00000414097.6:c.699-374C= ENSP00000404854.2:n.699-374C=
ENST00000517331.5:n.417-374C=
ENST00000517599.5:c.*305-374C= ENSP00000429172.1:n.*305-374C=
ENST00000518066.5:c.37-7089C= ENSP00000431057.1:n.37-7089C=
ENST00000518176.5:c.49-2482C= ENSP00000429007.1:n.49-2482C=
ENST00000519278.5:n.1795-374C=
ENST00000521414.5:n.160+184C=
ENST00000521664.1:n.449-374C=
ENST00000522377.5:c.*179-374C= ENSP00000429380.1:n.*179-374C=
ENST00000522476.5:c.501-374C= ENSP00000427894.1:n.501-374C=
ENST00000522665.5:n.22-374C=
ENST00000537882.2:c.456-374C= ENSP00000437443.1:n.456-374C=
NM_001135242.1:c.699-374C= NP_001128714.1:n.699-374C=
NM_001258432.1:c.501-374C= NP_001245361.1:n.501-374C=
NM_001258433.1:c.456-374C= NP_001245362.1:n.456-374C=
NM_006096.3:c.699-374C= , LRG_258t1:c.699-374C= NP_006087.2:n.699-374C=
XM_011516791.1:c.750-374C= XP_011515093.1:n.750-374C=
XM_011516792.1:c.132-374C= XP_011515094.1:n.132-374C=
XM_011516792.2:c.132-374C= XP_011515094.1:n.132-374C=
NM_001135242.2:c.699-374C= NP_001128714.1:n.699-374C=
NM_001258432.2:c.501-374C= NP_001245361.1:n.501-374C=
NM_001258433.2:c.456-374C= NP_001245362.1:n.456-374C=
NM_001374844.1:c.750-374C= NP_001361773.1:n.750-374C=
NM_001374845.1:c.699-374C= NP_001361774.1:n.699-374C=
NM_001374846.1:c.699-374C= NP_001361775.1:n.699-374C=
NM_001374847.1:c.501-374C= NP_001361776.1:n.501-374C=
NM_006096.4:c.699-374C= MANE Select NP_006087.2:n.699-374C=