Canonical Allele Identifier: CA372255183

Gene: NDRG1

Linked Data

• COSMIC: COSM454064
• MyVariant Identifiers: chr8:g.134260979C>G (hg19) ; chr8:g.133248736C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248736C>G , CM000670.2:g.133248736C>G	GRCh38
NC_000008.10:g.134260979C>G , CM000670.1:g.134260979C>G	GRCh37
NC_000008.9:g.134330161C>G	NCBI36
NG_007943.1:g.53520G>C , LRG_258:g.53520G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.734G>C MANE Select	ENSP00000319977.8:p.Gly245Ala
ENST00000537882.3:c.734G>C	ENSP00000437443.2:p.Gly245Ala
ENST00000675056.1:n.64G>C
ENST00000675068.1:c.36G>C
ENST00000675172.1:c.330G>C	ENSP00000502297.1:n.330G>C
ENST00000675273.1:n.93G>C
ENST00000675860.1:n.499G>C
ENST00000676444.1:n.765G>C
ENST00000323851.11:c.734G>C	ENSP00000319977.7:p.Gly245Ala
ENST00000414097.6:c.734G>C	ENSP00000404854.2:p.Gly245Ala
ENST00000517331.5:n.452G>C
ENST00000517599.5:c.*340G>C	ENSP00000429172.1:n.*340G>C
ENST00000518066.5:c.37-6680G>C	ENSP00000431057.1:n.37-6680G>C
ENST00000518176.5:c.49-2073G>C	ENSP00000429007.1:n.49-2073G>C
ENST00000519278.5:n.1830G>C
ENST00000521414.5:n.196G>C
ENST00000521664.1:n.484G>C
ENST00000522377.5:c.*214G>C	ENSP00000429380.1:n.*214G>C
ENST00000522476.5:c.536G>C	ENSP00000427894.1:p.Gly179Ala
ENST00000522665.5:n.57G>C
ENST00000537882.2:c.491G>C	ENSP00000437443.1:p.Gly164Ala
NM_001135242.1:c.734G>C	NP_001128714.1:p.Gly245Ala
NM_001258432.1:c.536G>C	NP_001245361.1:p.Gly179Ala
NM_001258433.1:c.491G>C	NP_001245362.1:p.Gly164Ala
NM_006096.3:c.734G>C , LRG_258t1:c.734G>C	NP_006087.2:p.Gly245Ala
XM_011516791.1:c.785G>C	XP_011515093.1:p.Gly262Ala
XM_011516792.1:c.167G>C	XP_011515094.1:p.Gly56Ala
XM_011516792.2:c.167G>C	XP_011515094.1:p.Gly56Ala
NM_001135242.2:c.734G>C	NP_001128714.1:p.Gly245Ala
NM_001258432.2:c.536G>C	NP_001245361.1:p.Gly179Ala
NM_001258433.2:c.491G>C	NP_001245362.1:p.Gly164Ala
NM_001374844.1:c.785G>C	NP_001361773.1:p.Gly262Ala
NM_001374845.1:c.734G>C	NP_001361774.1:p.Gly245Ala
NM_001374846.1:c.734G>C	NP_001361775.1:p.Gly245Ala
NM_001374847.1:c.536G>C	NP_001361776.1:p.Gly179Ala
NM_006096.4:c.734G>C MANE Select	NP_006087.2:p.Gly245Ala