Canonical Allele Identifier: CA1821167563

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133258374G= , CM000670.2:g.133258374G=	GRCh38
NC_000008.10:g.134270617G= , CM000670.1:g.134270617G=	GRCh37
NC_000008.9:g.134339799G=	NCBI36
NG_007943.1:g.43882C= , LRG_258:g.43882C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000323851.13:c.442C= MANE Select	ENSP00000319977.8:p.Arg148=
ENST00000519580.6:c.442C=	ENSP00000429272.1:p.Arg148=
ENST00000537882.3:c.442C=	ENSP00000437443.2:p.Arg148=
ENST00000676222.1:c.53C=
ENST00000676444.1:n.473C=
ENST00000323851.11:c.442C=	ENSP00000319977.7:p.Arg148=
ENST00000414097.6:c.442C=	ENSP00000404854.2:p.Arg148=
ENST00000517331.5:n.160C=
ENST00000517599.5:c.*48C=	ENSP00000429172.1:n.*48C=
ENST00000518010.5:n.526+794C=
ENST00000518066.5:c.37-16318C=	ENSP00000431057.1:n.37-16318C=
ENST00000518176.5:c.49-11711C=	ENSP00000429007.1:n.49-11711C=
ENST00000518480.5:c.244C=	ENSP00000428802.1:p.Arg82=
ENST00000519228.5:c.442C=	ENSP00000429994.1:p.Arg148=
ENST00000519580.5:c.442C=	ENSP00000429272.1:p.Arg148=
ENST00000520230.5:c.493C=	ENSP00000428345.1:p.Arg165=
ENST00000522377.5:c.442C=	ENSP00000429380.1:p.Arg148=
ENST00000522476.5:c.244C=	ENSP00000427894.1:p.Arg82=
ENST00000522890.5:c.442C=	ENSP00000428384.1:p.Arg148=
ENST00000537882.2:c.199C=	ENSP00000437443.1:p.Arg67=
NM_001135242.1:c.442C=	NP_001128714.1:p.Arg148=
NM_001258432.1:c.244C=	NP_001245361.1:p.Arg82=
NM_001258433.1:c.199C=	NP_001245362.1:p.Arg67=
NM_006096.3:c.442C= , LRG_258t1:c.442C=	NP_006087.2:p.Arg148=
XM_011516791.1:c.442C=	XP_011515093.1:p.Arg148=
NM_001135242.2:c.442C=	NP_001128714.1:p.Arg148=
NM_001258432.2:c.244C=	NP_001245361.1:p.Arg82=
NM_001258433.2:c.199C=	NP_001245362.1:p.Arg67=
NM_001374844.1:c.442C=	NP_001361773.1:p.Arg148=
NM_001374845.1:c.442C=	NP_001361774.1:p.Arg148=
NM_001374846.1:c.442C=	NP_001361775.1:p.Arg148=
NM_001374847.1:c.244C=	NP_001361776.1:p.Arg82=
NM_006096.4:c.442C= MANE Select	NP_006087.2:p.Arg148=