Canonical Allele Identifier: CA1821166349

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248766C= , CM000670.2:g.133248766C=	GRCh38
NC_000008.10:g.134261009C= , CM000670.1:g.134261009C=	GRCh37
NC_000008.9:g.134330191C=	NCBI36
NG_007943.1:g.53490G= , LRG_258:g.53490G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.704G= MANE Select	ENSP00000319977.8:p.Arg235=
ENST00000537882.3:c.704G=	ENSP00000437443.2:p.Arg235=
ENST00000675056.1:n.34G=
ENST00000675068.1:c.6G=
ENST00000675172.1:c.300G=	ENSP00000502297.1:n.300G=
ENST00000675273.1:n.63G=
ENST00000675860.1:n.469G=
ENST00000676444.1:n.735G=
ENST00000323851.11:c.704G=	ENSP00000319977.7:p.Arg235=
ENST00000414097.6:c.704G=	ENSP00000404854.2:p.Arg235=
ENST00000517331.5:n.422G=
ENST00000517599.5:c.*310G=	ENSP00000429172.1:n.*310G=
ENST00000518066.5:c.37-6710G=	ENSP00000431057.1:n.37-6710G=
ENST00000518176.5:c.49-2103G=	ENSP00000429007.1:n.49-2103G=
ENST00000519278.5:n.1800G=
ENST00000521414.5:n.166G=
ENST00000521664.1:n.454G=
ENST00000522377.5:c.*184G=	ENSP00000429380.1:n.*184G=
ENST00000522476.5:c.506G=	ENSP00000427894.1:p.Arg169=
ENST00000522665.5:n.27G=
ENST00000537882.2:c.461G=	ENSP00000437443.1:p.Arg154=
NM_001135242.1:c.704G=	NP_001128714.1:p.Arg235=
NM_001258432.1:c.506G=	NP_001245361.1:p.Arg169=
NM_001258433.1:c.461G=	NP_001245362.1:p.Arg154=
NM_006096.3:c.704G= , LRG_258t1:c.704G=	NP_006087.2:p.Arg235=
XM_011516791.1:c.755G=	XP_011515093.1:p.Arg252=
XM_011516792.1:c.137G=	XP_011515094.1:p.Arg46=
XM_011516792.2:c.137G=	XP_011515094.1:p.Arg46=
NM_001135242.2:c.704G=	NP_001128714.1:p.Arg235=
NM_001258432.2:c.506G=	NP_001245361.1:p.Arg169=
NM_001258433.2:c.461G=	NP_001245362.1:p.Arg154=
NM_001374844.1:c.755G=	NP_001361773.1:p.Arg252=
NM_001374845.1:c.704G=	NP_001361774.1:p.Arg235=
NM_001374846.1:c.704G=	NP_001361775.1:p.Arg235=
NM_001374847.1:c.506G=	NP_001361776.1:p.Arg169=
NM_006096.4:c.704G= MANE Select	NP_006087.2:p.Arg235=