Canonical Allele Identifier: CA1821166327
Gene: NDRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133248750C= , CM000670.2:g.133248750C= GRCh38
NC_000008.10:g.134260993C= , CM000670.1:g.134260993C= GRCh37
NC_000008.9:g.134330175C= NCBI36
NG_007943.1:g.53506G= , LRG_258:g.53506G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.720G= MANE Select ENSP00000319977.8:p.Glu240=
ENST00000537882.3:c.720G= ENSP00000437443.2:p.Glu240=
ENST00000675056.1:n.50G=
ENST00000675068.1:c.22G=
ENST00000675172.1:c.316G= ENSP00000502297.1:n.316G=
ENST00000675273.1:n.79G=
ENST00000675860.1:n.485G=
ENST00000676444.1:n.751G=
ENST00000323851.11:c.720G= ENSP00000319977.7:p.Glu240=
ENST00000414097.6:c.720G= ENSP00000404854.2:p.Glu240=
ENST00000517331.5:n.438G=
ENST00000517599.5:c.*326G= ENSP00000429172.1:n.*326G=
ENST00000518066.5:c.37-6694G= ENSP00000431057.1:n.37-6694G=
ENST00000518176.5:c.49-2087G= ENSP00000429007.1:n.49-2087G=
ENST00000519278.5:n.1816G=
ENST00000521414.5:n.182G=
ENST00000521664.1:n.470G=
ENST00000522377.5:c.*200G= ENSP00000429380.1:n.*200G=
ENST00000522476.5:c.522G= ENSP00000427894.1:p.Glu174=
ENST00000522665.5:n.43G=
ENST00000537882.2:c.477G= ENSP00000437443.1:p.Glu159=
NM_001135242.1:c.720G= NP_001128714.1:p.Glu240=
NM_001258432.1:c.522G= NP_001245361.1:p.Glu174=
NM_001258433.1:c.477G= NP_001245362.1:p.Glu159=
NM_006096.3:c.720G= , LRG_258t1:c.720G= NP_006087.2:p.Glu240=
XM_011516791.1:c.771G= XP_011515093.1:p.Glu257=
XM_011516792.1:c.153G= XP_011515094.1:p.Glu51=
XM_011516792.2:c.153G= XP_011515094.1:p.Glu51=
NM_001135242.2:c.720G= NP_001128714.1:p.Glu240=
NM_001258432.2:c.522G= NP_001245361.1:p.Glu174=
NM_001258433.2:c.477G= NP_001245362.1:p.Glu159=
NM_001374844.1:c.771G= NP_001361773.1:p.Glu257=
NM_001374845.1:c.720G= NP_001361774.1:p.Glu240=
NM_001374846.1:c.720G= NP_001361775.1:p.Glu240=
NM_001374847.1:c.522G= NP_001361776.1:p.Glu174=
NM_006096.4:c.720G= MANE Select NP_006087.2:p.Glu240=