Canonical Allele Identifier: CA463019428

Gene: NDRG1

Linked Data

• ClinVar Variation Id: 1628357
• ClinVar RCV Id: RCV002114413
• dbSNP Id: rs1855837777
• MyVariant Identifiers: chr8:g.134260963G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248720G>C , CM000670.2:g.133248720G>C	GRCh38
NC_000008.10:g.134260963G>C , CM000670.1:g.134260963G>C	GRCh37
NC_000008.9:g.134330145G>C	NCBI36
NG_007943.1:g.53536C>G , LRG_258:g.53536C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.750C>G MANE Select	ENSP00000319977.8:p.Thr250=
ENST00000537882.3:c.750C>G	ENSP00000437443.2:p.Thr250=
ENST00000675056.1:n.80C>G
ENST00000675068.1:c.52C>G
ENST00000675172.1:c.346C>G	ENSP00000502297.1:n.346C>G
ENST00000675273.1:n.109C>G
ENST00000675860.1:n.515C>G
ENST00000323851.11:c.750C>G	ENSP00000319977.7:p.Thr250=
ENST00000414097.6:c.750C>G	ENSP00000404854.2:p.Thr250=
ENST00000517331.5:n.468C>G
ENST00000517599.5:c.*356C>G	ENSP00000429172.1:n.*356C>G
ENST00000518066.5:c.37-6664C>G	ENSP00000431057.1:n.37-6664C>G
ENST00000518176.5:c.49-2057C>G	ENSP00000429007.1:n.49-2057C>G
ENST00000519278.5:n.1846C>G
ENST00000521414.5:n.212C>G
ENST00000521664.1:n.500C>G
ENST00000522377.5:c.*230C>G	ENSP00000429380.1:n.*230C>G
ENST00000522476.5:c.552C>G	ENSP00000427894.1:p.Thr184=
ENST00000522665.5:n.73C>G
ENST00000537882.2:c.507C>G	ENSP00000437443.1:p.Thr169=
NM_001135242.1:c.750C>G	NP_001128714.1:p.Thr250=
NM_001258432.1:c.552C>G	NP_001245361.1:p.Thr184=
NM_001258433.1:c.507C>G	NP_001245362.1:p.Thr169=
NM_006096.3:c.750C>G , LRG_258t1:c.750C>G	NP_006087.2:p.Thr250=
XM_011516791.1:c.801C>G	XP_011515093.1:p.Thr267=
XM_011516792.1:c.183C>G	XP_011515094.1:p.Thr61=
XM_011516792.2:c.183C>G	XP_011515094.1:p.Thr61=
NM_001135242.2:c.750C>G	NP_001128714.1:p.Thr250=
NM_001258432.2:c.552C>G	NP_001245361.1:p.Thr184=
NM_001258433.2:c.507C>G	NP_001245362.1:p.Thr169=
NM_001374844.1:c.801C>G	NP_001361773.1:p.Thr267=
NM_001374845.1:c.750C>G	NP_001361774.1:p.Thr250=
NM_001374846.1:c.750C>G	NP_001361775.1:p.Thr250=
NM_001374847.1:c.552C>G	NP_001361776.1:p.Thr184=
NM_006096.4:c.750C>G MANE Select	NP_006087.2:p.Thr250=