Canonical Allele Identifier: CA1821166309

Gene: NDRG1

Linked Data

• dbSNP Id: rs1855841324

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248746del , CM000670.2:g.133248746del	GRCh38
NC_000008.10:g.134260989del , CM000670.1:g.134260989del	GRCh37
NC_000008.9:g.134330171del	NCBI36
NG_007943.1:g.53511del , LRG_258:g.53511del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.725del MANE Select	ENSP00000319977.8:p.Pro242GlnfsTer?
ENST00000537882.3:c.725del	ENSP00000437443.2:p.Pro242GlnfsTer?
ENST00000675056.1:n.55del
ENST00000675068.1:c.27del
ENST00000675172.1:c.321del	ENSP00000502297.1:n.321del
ENST00000675273.1:n.84del
ENST00000675860.1:n.490del
ENST00000676444.1:n.756del
ENST00000323851.11:c.725del	ENSP00000319977.7:p.Pro242GlnfsTer?
ENST00000414097.6:c.725del	ENSP00000404854.2:p.Pro242GlnfsTer?
ENST00000517331.5:n.443del
ENST00000517599.5:c.*331del	ENSP00000429172.1:n.*331del
ENST00000518066.5:c.37-6689del	ENSP00000431057.1:n.37-6689del
ENST00000518176.5:c.49-2082del	ENSP00000429007.1:n.49-2082del
ENST00000519278.5:n.1821del
ENST00000521414.5:n.187del
ENST00000521664.1:n.475del
ENST00000522377.5:c.*205del	ENSP00000429380.1:n.*205del
ENST00000522476.5:c.527del	ENSP00000427894.1:p.Pro176GlnfsTer?
ENST00000522665.5:n.48del
ENST00000537882.2:c.482del	ENSP00000437443.1:p.Pro161GlnfsTer?
NM_001135242.1:c.725del	NP_001128714.1:p.Pro242GlnfsTer?
NM_001258432.1:c.527del	NP_001245361.1:p.Pro176GlnfsTer?
NM_001258433.1:c.482del	NP_001245362.1:p.Pro161GlnfsTer?
NM_006096.3:c.725del , LRG_258t1:c.725del	NP_006087.2:p.Pro242GlnfsTer?
XM_011516791.1:c.776del	XP_011515093.1:p.Pro259GlnfsTer?
XM_011516792.1:c.158del	XP_011515094.1:p.Pro53GlnfsTer?
XM_011516792.2:c.158del	XP_011515094.1:p.Pro53GlnfsTer?
NM_001135242.2:c.725del	NP_001128714.1:p.Pro242GlnfsTer?
NM_001258432.2:c.527del	NP_001245361.1:p.Pro176GlnfsTer?
NM_001258433.2:c.482del	NP_001245362.1:p.Pro161GlnfsTer?
NM_001374844.1:c.776del	NP_001361773.1:p.Pro259GlnfsTer?
NM_001374845.1:c.725del	NP_001361774.1:p.Pro242GlnfsTer?
NM_001374846.1:c.725del	NP_001361775.1:p.Pro242GlnfsTer?
NM_001374847.1:c.527del	NP_001361776.1:p.Pro176GlnfsTer?
NM_006096.4:c.725del MANE Select	NP_006087.2:p.Pro242GlnfsTer?