Canonical Allele Identifier: CA1821166237

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248726T= , CM000670.2:g.133248726T=	GRCh38
NC_000008.10:g.134260969T= , CM000670.1:g.134260969T=	GRCh37
NC_000008.9:g.134330151T=	NCBI36
NG_007943.1:g.53530A= , LRG_258:g.53530A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.744A= MANE Select	ENSP00000319977.8:p.Thr248=
ENST00000537882.3:c.744A=	ENSP00000437443.2:p.Thr248=
ENST00000675056.1:n.74A=
ENST00000675068.1:c.46A=
ENST00000675172.1:c.340A=	ENSP00000502297.1:n.340A=
ENST00000675273.1:n.103A=
ENST00000675860.1:n.509A=
ENST00000676444.1:n.775A=
ENST00000323851.11:c.744A=	ENSP00000319977.7:p.Thr248=
ENST00000414097.6:c.744A=	ENSP00000404854.2:p.Thr248=
ENST00000517331.5:n.462A=
ENST00000517599.5:c.*350A=	ENSP00000429172.1:n.*350A=
ENST00000518066.5:c.37-6670A=	ENSP00000431057.1:n.37-6670A=
ENST00000518176.5:c.49-2063A=	ENSP00000429007.1:n.49-2063A=
ENST00000519278.5:n.1840A=
ENST00000521414.5:n.206A=
ENST00000521664.1:n.494A=
ENST00000522377.5:c.*224A=	ENSP00000429380.1:n.*224A=
ENST00000522476.5:c.546A=	ENSP00000427894.1:p.Thr182=
ENST00000522665.5:n.67A=
ENST00000537882.2:c.501A=	ENSP00000437443.1:p.Thr167=
NM_001135242.1:c.744A=	NP_001128714.1:p.Thr248=
NM_001258432.1:c.546A=	NP_001245361.1:p.Thr182=
NM_001258433.1:c.501A=	NP_001245362.1:p.Thr167=
NM_006096.3:c.744A= , LRG_258t1:c.744A=	NP_006087.2:p.Thr248=
XM_011516791.1:c.795A=	XP_011515093.1:p.Thr265=
XM_011516792.1:c.177A=	XP_011515094.1:p.Thr59=
XM_011516792.2:c.177A=	XP_011515094.1:p.Thr59=
NM_001135242.2:c.744A=	NP_001128714.1:p.Thr248=
NM_001258432.2:c.546A=	NP_001245361.1:p.Thr182=
NM_001258433.2:c.501A=	NP_001245362.1:p.Thr167=
NM_001374844.1:c.795A=	NP_001361773.1:p.Thr265=
NM_001374845.1:c.744A=	NP_001361774.1:p.Thr248=
NM_001374846.1:c.744A=	NP_001361775.1:p.Thr248=
NM_001374847.1:c.546A=	NP_001361776.1:p.Thr182=
NM_006096.4:c.744A= MANE Select	NP_006087.2:p.Thr248=