Canonical Allele Identifier: CA1821166265

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248731G= , CM000670.2:g.133248731G=	GRCh38
NC_000008.10:g.134260974G= , CM000670.1:g.134260974G=	GRCh37
NC_000008.9:g.134330156G=	NCBI36
NG_007943.1:g.53525C= , LRG_258:g.53525C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.739C= MANE Select	ENSP00000319977.8:p.His247=
ENST00000537882.3:c.739C=	ENSP00000437443.2:p.His247=
ENST00000675056.1:n.69C=
ENST00000675068.1:c.41C=
ENST00000675172.1:c.335C=	ENSP00000502297.1:n.335C=
ENST00000675273.1:n.98C=
ENST00000675860.1:n.504C=
ENST00000676444.1:n.770C=
ENST00000323851.11:c.739C=	ENSP00000319977.7:p.His247=
ENST00000414097.6:c.739C=	ENSP00000404854.2:p.His247=
ENST00000517331.5:n.457C=
ENST00000517599.5:c.*345C=	ENSP00000429172.1:n.*345C=
ENST00000518066.5:c.37-6675C=	ENSP00000431057.1:n.37-6675C=
ENST00000518176.5:c.49-2068C=	ENSP00000429007.1:n.49-2068C=
ENST00000519278.5:n.1835C=
ENST00000521414.5:n.201C=
ENST00000521664.1:n.489C=
ENST00000522377.5:c.*219C=	ENSP00000429380.1:n.*219C=
ENST00000522476.5:c.541C=	ENSP00000427894.1:p.His181=
ENST00000522665.5:n.62C=
ENST00000537882.2:c.496C=	ENSP00000437443.1:p.His166=
NM_001135242.1:c.739C=	NP_001128714.1:p.His247=
NM_001258432.1:c.541C=	NP_001245361.1:p.His181=
NM_001258433.1:c.496C=	NP_001245362.1:p.His166=
NM_006096.3:c.739C= , LRG_258t1:c.739C=	NP_006087.2:p.His247=
XM_011516791.1:c.790C=	XP_011515093.1:p.His264=
XM_011516792.1:c.172C=	XP_011515094.1:p.His58=
XM_011516792.2:c.172C=	XP_011515094.1:p.His58=
NM_001135242.2:c.739C=	NP_001128714.1:p.His247=
NM_001258432.2:c.541C=	NP_001245361.1:p.His181=
NM_001258433.2:c.496C=	NP_001245362.1:p.His166=
NM_001374844.1:c.790C=	NP_001361773.1:p.His264=
NM_001374845.1:c.739C=	NP_001361774.1:p.His247=
NM_001374846.1:c.739C=	NP_001361775.1:p.His247=
NM_001374847.1:c.541C=	NP_001361776.1:p.His181=
NM_006096.4:c.739C= MANE Select	NP_006087.2:p.His247=