Canonical Allele Identifier: CA1821166935
Gene: NDRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133249082C= , CM000670.2:g.133249082C= GRCh38
NC_000008.10:g.134261325C= , CM000670.1:g.134261325C= GRCh37
NC_000008.9:g.134330507C= NCBI36
NG_007943.1:g.53174G= , LRG_258:g.53174G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.699-311G= MANE Select ENSP00000319977.8:n.699-311G=
ENST00000537882.3:c.699-311G= ENSP00000437443.2:n.699-311G=
ENST00000675056.1:n.28+298G=
ENST00000675172.1:c.295-311G= ENSP00000502297.1:n.295-311G=
ENST00000675273.1:n.58-311G=
ENST00000675860.1:n.464-311G=
ENST00000676444.1:n.730-311G=
ENST00000323851.11:c.699-311G= ENSP00000319977.7:n.699-311G=
ENST00000414097.6:c.699-311G= ENSP00000404854.2:n.699-311G=
ENST00000517331.5:n.417-311G=
ENST00000517599.5:c.*305-311G= ENSP00000429172.1:n.*305-311G=
ENST00000518066.5:c.37-7026G= ENSP00000431057.1:n.37-7026G=
ENST00000518176.5:c.49-2419G= ENSP00000429007.1:n.49-2419G=
ENST00000519278.5:n.1795-311G=
ENST00000521414.5:n.160+247G=
ENST00000521664.1:n.449-311G=
ENST00000522377.5:c.*179-311G= ENSP00000429380.1:n.*179-311G=
ENST00000522476.5:c.501-311G= ENSP00000427894.1:n.501-311G=
ENST00000522665.5:n.22-311G=
ENST00000537882.2:c.456-311G= ENSP00000437443.1:n.456-311G=
NM_001135242.1:c.699-311G= NP_001128714.1:n.699-311G=
NM_001258432.1:c.501-311G= NP_001245361.1:n.501-311G=
NM_001258433.1:c.456-311G= NP_001245362.1:n.456-311G=
NM_006096.3:c.699-311G= , LRG_258t1:c.699-311G= NP_006087.2:n.699-311G=
XM_011516791.1:c.750-311G= XP_011515093.1:n.750-311G=
XM_011516792.1:c.132-311G= XP_011515094.1:n.132-311G=
XM_011516792.2:c.132-311G= XP_011515094.1:n.132-311G=
NM_001135242.2:c.699-311G= NP_001128714.1:n.699-311G=
NM_001258432.2:c.501-311G= NP_001245361.1:n.501-311G=
NM_001258433.2:c.456-311G= NP_001245362.1:n.456-311G=
NM_001374844.1:c.750-311G= NP_001361773.1:n.750-311G=
NM_001374845.1:c.699-311G= NP_001361774.1:n.699-311G=
NM_001374846.1:c.699-311G= NP_001361775.1:n.699-311G=
NM_001374847.1:c.501-311G= NP_001361776.1:n.501-311G=
NM_006096.4:c.699-311G= MANE Select NP_006087.2:n.699-311G=