Canonical Allele Identifier: CA372255163

Gene: NDRG1

Linked Data

• MyVariant Identifiers: chr8:g.134260970G>T (hg19) ; chr8:g.133248727G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248727G>T , CM000670.2:g.133248727G>T	GRCh38
NC_000008.10:g.134260970G>T , CM000670.1:g.134260970G>T	GRCh37
NC_000008.9:g.134330152G>T	NCBI36
NG_007943.1:g.53529C>A , LRG_258:g.53529C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.743C>A MANE Select	ENSP00000319977.8:p.Thr248Lys
ENST00000537882.3:c.743C>A	ENSP00000437443.2:p.Thr248Lys
ENST00000675056.1:n.73C>A
ENST00000675068.1:c.45C>A
ENST00000675172.1:c.339C>A	ENSP00000502297.1:n.339C>A
ENST00000675273.1:n.102C>A
ENST00000675860.1:n.508C>A
ENST00000676444.1:n.774C>A
ENST00000323851.11:c.743C>A	ENSP00000319977.7:p.Thr248Lys
ENST00000414097.6:c.743C>A	ENSP00000404854.2:p.Thr248Lys
ENST00000517331.5:n.461C>A
ENST00000517599.5:c.*349C>A	ENSP00000429172.1:n.*349C>A
ENST00000518066.5:c.37-6671C>A	ENSP00000431057.1:n.37-6671C>A
ENST00000518176.5:c.49-2064C>A	ENSP00000429007.1:n.49-2064C>A
ENST00000519278.5:n.1839C>A
ENST00000521414.5:n.205C>A
ENST00000521664.1:n.493C>A
ENST00000522377.5:c.*223C>A	ENSP00000429380.1:n.*223C>A
ENST00000522476.5:c.545C>A	ENSP00000427894.1:p.Thr182Lys
ENST00000522665.5:n.66C>A
ENST00000537882.2:c.500C>A	ENSP00000437443.1:p.Thr167Lys
NM_001135242.1:c.743C>A	NP_001128714.1:p.Thr248Lys
NM_001258432.1:c.545C>A	NP_001245361.1:p.Thr182Lys
NM_001258433.1:c.500C>A	NP_001245362.1:p.Thr167Lys
NM_006096.3:c.743C>A , LRG_258t1:c.743C>A	NP_006087.2:p.Thr248Lys
XM_011516791.1:c.794C>A	XP_011515093.1:p.Thr265Lys
XM_011516792.1:c.176C>A	XP_011515094.1:p.Thr59Lys
XM_011516792.2:c.176C>A	XP_011515094.1:p.Thr59Lys
NM_001135242.2:c.743C>A	NP_001128714.1:p.Thr248Lys
NM_001258432.2:c.545C>A	NP_001245361.1:p.Thr182Lys
NM_001258433.2:c.500C>A	NP_001245362.1:p.Thr167Lys
NM_001374844.1:c.794C>A	NP_001361773.1:p.Thr265Lys
NM_001374845.1:c.743C>A	NP_001361774.1:p.Thr248Lys
NM_001374846.1:c.743C>A	NP_001361775.1:p.Thr248Lys
NM_001374847.1:c.545C>A	NP_001361776.1:p.Thr182Lys
NM_006096.4:c.743C>A MANE Select	NP_006087.2:p.Thr248Lys