Canonical Allele Identifier: CA1821166316
Gene: NDRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133248746G= , CM000670.2:g.133248746G= GRCh38
NC_000008.10:g.134260989G= , CM000670.1:g.134260989G= GRCh37
NC_000008.9:g.134330171G= NCBI36
NG_007943.1:g.53510C= , LRG_258:g.53510C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.724C= MANE Select ENSP00000319977.8:p.Pro242=
ENST00000537882.3:c.724C= ENSP00000437443.2:p.Pro242=
ENST00000675056.1:n.54C=
ENST00000675068.1:c.26C=
ENST00000675172.1:c.320C= ENSP00000502297.1:n.320C=
ENST00000675273.1:n.83C=
ENST00000675860.1:n.489C=
ENST00000676444.1:n.755C=
ENST00000323851.11:c.724C= ENSP00000319977.7:p.Pro242=
ENST00000414097.6:c.724C= ENSP00000404854.2:p.Pro242=
ENST00000517331.5:n.442C=
ENST00000517599.5:c.*330C= ENSP00000429172.1:n.*330C=
ENST00000518066.5:c.37-6690C= ENSP00000431057.1:n.37-6690C=
ENST00000518176.5:c.49-2083C= ENSP00000429007.1:n.49-2083C=
ENST00000519278.5:n.1820C=
ENST00000521414.5:n.186C=
ENST00000521664.1:n.474C=
ENST00000522377.5:c.*204C= ENSP00000429380.1:n.*204C=
ENST00000522476.5:c.526C= ENSP00000427894.1:p.Pro176=
ENST00000522665.5:n.47C=
ENST00000537882.2:c.481C= ENSP00000437443.1:p.Pro161=
NM_001135242.1:c.724C= NP_001128714.1:p.Pro242=
NM_001258432.1:c.526C= NP_001245361.1:p.Pro176=
NM_001258433.1:c.481C= NP_001245362.1:p.Pro161=
NM_006096.3:c.724C= , LRG_258t1:c.724C= NP_006087.2:p.Pro242=
XM_011516791.1:c.775C= XP_011515093.1:p.Pro259=
XM_011516792.1:c.157C= XP_011515094.1:p.Pro53=
XM_011516792.2:c.157C= XP_011515094.1:p.Pro53=
NM_001135242.2:c.724C= NP_001128714.1:p.Pro242=
NM_001258432.2:c.526C= NP_001245361.1:p.Pro176=
NM_001258433.2:c.481C= NP_001245362.1:p.Pro161=
NM_001374844.1:c.775C= NP_001361773.1:p.Pro259=
NM_001374845.1:c.724C= NP_001361774.1:p.Pro242=
NM_001374846.1:c.724C= NP_001361775.1:p.Pro242=
NM_001374847.1:c.526C= NP_001361776.1:p.Pro176=
NM_006096.4:c.724C= MANE Select NP_006087.2:p.Pro242=