Canonical Allele Identifier: CA2579257266

Gene: NDRG1

Linked Data

• ClinVar Variation Id: 2804373
• ClinVar RCV Id: RCV003745937

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248790del , CM000670.2:g.133248790del	GRCh38
NC_000008.10:g.134261033del , CM000670.1:g.134261033del	GRCh37
NC_000008.9:g.134330215del	NCBI36
NG_007943.1:g.53466del , LRG_258:g.53466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.699-19del MANE Select	ENSP00000319977.8:n.699-19del
ENST00000537882.3:c.699-19del	ENSP00000437443.2:n.699-19del
ENST00000675056.1:n.29-19del
ENST00000675172.1:c.295-19del	ENSP00000502297.1:n.295-19del
ENST00000675273.1:n.58-19del
ENST00000675860.1:n.464-19del
ENST00000676444.1:n.730-19del
ENST00000323851.11:c.699-19del	ENSP00000319977.7:n.699-19del
ENST00000414097.6:c.699-19del	ENSP00000404854.2:n.699-19del
ENST00000517331.5:n.417-19del
ENST00000517599.5:c.*305-19del	ENSP00000429172.1:n.*305-19del
ENST00000518066.5:c.37-6734del	ENSP00000431057.1:n.37-6734del
ENST00000518176.5:c.49-2127del	ENSP00000429007.1:n.49-2127del
ENST00000519278.5:n.1795-19del
ENST00000521414.5:n.161-19del
ENST00000521664.1:n.449-19del
ENST00000522377.5:c.*179-19del	ENSP00000429380.1:n.*179-19del
ENST00000522476.5:c.501-19del	ENSP00000427894.1:n.501-19del
ENST00000522665.5:n.22-19del
ENST00000537882.2:c.456-19del	ENSP00000437443.1:n.456-19del
NM_001135242.1:c.699-19del	NP_001128714.1:n.699-19del
NM_001258432.1:c.501-19del	NP_001245361.1:n.501-19del
NM_001258433.1:c.456-19del	NP_001245362.1:n.456-19del
NM_006096.3:c.699-19del , LRG_258t1:c.699-19del	NP_006087.2:n.699-19del
XM_011516791.1:c.750-19del	XP_011515093.1:n.750-19del
XM_011516792.1:c.132-19del	XP_011515094.1:n.132-19del
XM_011516792.2:c.132-19del	XP_011515094.1:n.132-19del
NM_001135242.2:c.699-19del	NP_001128714.1:n.699-19del
NM_001258432.2:c.501-19del	NP_001245361.1:n.501-19del
NM_001258433.2:c.456-19del	NP_001245362.1:n.456-19del
NM_001374844.1:c.750-19del	NP_001361773.1:n.750-19del
NM_001374845.1:c.699-19del	NP_001361774.1:n.699-19del
NM_001374846.1:c.699-19del	NP_001361775.1:n.699-19del
NM_001374847.1:c.501-19del	NP_001361776.1:n.501-19del
NM_006096.4:c.699-19del MANE Select	NP_006087.2:n.699-19del