Canonical Allele Identifier: CA1821166321

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248748C= , CM000670.2:g.133248748C=	GRCh38
NC_000008.10:g.134260991C= , CM000670.1:g.134260991C=	GRCh37
NC_000008.9:g.134330173C=	NCBI36
NG_007943.1:g.53508G= , LRG_258:g.53508G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.722G= MANE Select	ENSP00000319977.8:p.Arg241=
ENST00000537882.3:c.722G=	ENSP00000437443.2:p.Arg241=
ENST00000675056.1:n.52G=
ENST00000675068.1:c.24G=
ENST00000675172.1:c.318G=	ENSP00000502297.1:n.318G=
ENST00000675273.1:n.81G=
ENST00000675860.1:n.487G=
ENST00000676444.1:n.753G=
ENST00000323851.11:c.722G=	ENSP00000319977.7:p.Arg241=
ENST00000414097.6:c.722G=	ENSP00000404854.2:p.Arg241=
ENST00000517331.5:n.440G=
ENST00000517599.5:c.*328G=	ENSP00000429172.1:n.*328G=
ENST00000518066.5:c.37-6692G=	ENSP00000431057.1:n.37-6692G=
ENST00000518176.5:c.49-2085G=	ENSP00000429007.1:n.49-2085G=
ENST00000519278.5:n.1818G=
ENST00000521414.5:n.184G=
ENST00000521664.1:n.472G=
ENST00000522377.5:c.*202G=	ENSP00000429380.1:n.*202G=
ENST00000522476.5:c.524G=	ENSP00000427894.1:p.Arg175=
ENST00000522665.5:n.45G=
ENST00000537882.2:c.479G=	ENSP00000437443.1:p.Arg160=
NM_001135242.1:c.722G=	NP_001128714.1:p.Arg241=
NM_001258432.1:c.524G=	NP_001245361.1:p.Arg175=
NM_001258433.1:c.479G=	NP_001245362.1:p.Arg160=
NM_006096.3:c.722G= , LRG_258t1:c.722G=	NP_006087.2:p.Arg241=
XM_011516791.1:c.773G=	XP_011515093.1:p.Arg258=
XM_011516792.1:c.155G=	XP_011515094.1:p.Arg52=
XM_011516792.2:c.155G=	XP_011515094.1:p.Arg52=
NM_001135242.2:c.722G=	NP_001128714.1:p.Arg241=
NM_001258432.2:c.524G=	NP_001245361.1:p.Arg175=
NM_001258433.2:c.479G=	NP_001245362.1:p.Arg160=
NM_001374844.1:c.773G=	NP_001361773.1:p.Arg258=
NM_001374845.1:c.722G=	NP_001361774.1:p.Arg241=
NM_001374846.1:c.722G=	NP_001361775.1:p.Arg241=
NM_001374847.1:c.524G=	NP_001361776.1:p.Arg175=
NM_006096.4:c.722G= MANE Select	NP_006087.2:p.Arg241=