Canonical Allele Identifier: CA4886626
Gene: NDRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476848
dbSNP Id: rs772268356

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133248767G>A , CM000670.2:g.133248767G>A GRCh38
NC_000008.10:g.134261010G>A , CM000670.1:g.134261010G>A GRCh37
NC_000008.9:g.134330192G>A NCBI36
NG_007943.1:g.53489C>T , LRG_258:g.53489C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323851.13:c.703C>T MANE Select ENSP00000319977.8:p.Arg235Cys
ENST00000537882.3:c.703C>T ENSP00000437443.2:p.Arg235Cys
ENST00000675056.1:n.33C>T
ENST00000675068.1:c.5C>T
ENST00000675172.1:c.299C>T ENSP00000502297.1:n.299C>T
ENST00000675273.1:n.62C>T
ENST00000675860.1:n.468C>T
ENST00000676444.1:n.734C>T
ENST00000323851.11:c.703C>T ENSP00000319977.7:p.Arg235Cys
ENST00000414097.6:c.703C>T ENSP00000404854.2:p.Arg235Cys
ENST00000517331.5:n.421C>T
ENST00000517599.5:c.*309C>T ENSP00000429172.1:n.*309C>T
ENST00000518066.5:c.37-6711C>T ENSP00000431057.1:n.37-6711C>T
ENST00000518176.5:c.49-2104C>T ENSP00000429007.1:n.49-2104C>T
ENST00000519278.5:n.1799C>T
ENST00000521414.5:n.165C>T
ENST00000521664.1:n.453C>T
ENST00000522377.5:c.*183C>T ENSP00000429380.1:n.*183C>T
ENST00000522476.5:c.505C>T ENSP00000427894.1:p.Arg169Cys
ENST00000522665.5:n.26C>T
ENST00000537882.2:c.460C>T ENSP00000437443.1:p.Arg154Cys
NM_001135242.1:c.703C>T NP_001128714.1:p.Arg235Cys
NM_001258432.1:c.505C>T NP_001245361.1:p.Arg169Cys
NM_001258433.1:c.460C>T NP_001245362.1:p.Arg154Cys
NM_006096.3:c.703C>T , LRG_258t1:c.703C>T NP_006087.2:p.Arg235Cys
XM_011516791.1:c.754C>T XP_011515093.1:p.Arg252Cys
XM_011516792.1:c.136C>T XP_011515094.1:p.Arg46Cys
XM_011516792.2:c.136C>T XP_011515094.1:p.Arg46Cys
NM_001135242.2:c.703C>T NP_001128714.1:p.Arg235Cys
NM_001258432.2:c.505C>T NP_001245361.1:p.Arg169Cys
NM_001258433.2:c.460C>T NP_001245362.1:p.Arg154Cys
NM_001374844.1:c.754C>T NP_001361773.1:p.Arg252Cys
NM_001374845.1:c.703C>T NP_001361774.1:p.Arg235Cys
NM_001374846.1:c.703C>T NP_001361775.1:p.Arg235Cys
NM_001374847.1:c.505C>T NP_001361776.1:p.Arg169Cys
NM_006096.4:c.703C>T MANE Select NP_006087.2:p.Arg235Cys