Canonical Allele Identifier: CA1821166008

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248624G= , CM000670.2:g.133248624G=	GRCh38
NC_000008.10:g.134260867G= , CM000670.1:g.134260867G=	GRCh37
NC_000008.9:g.134330049G=	NCBI36
NG_007943.1:g.53632C= , LRG_258:g.53632C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.755+91C= MANE Select	ENSP00000319977.8:n.755+91C=
ENST00000537882.3:c.755+91C=	ENSP00000437443.2:n.755+91C=
ENST00000675068.1:c.57+91C=
ENST00000675860.1:n.520+91C=
ENST00000323851.11:c.755+91C=	ENSP00000319977.7:n.755+91C=
ENST00000414097.6:c.755+91C=	ENSP00000404854.2:n.755+91C=
ENST00000517331.5:n.473+91C=
ENST00000517599.5:c.*361+91C=	ENSP00000429172.1:n.*361+91C=
ENST00000518066.5:c.37-6568C=	ENSP00000431057.1:n.37-6568C=
ENST00000518176.5:c.49-1961C=	ENSP00000429007.1:n.49-1961C=
ENST00000519278.5:n.1851+91C=
ENST00000521414.5:n.217+91C=
ENST00000521664.1:n.505+91C=
ENST00000522377.5:c.*235+91C=	ENSP00000429380.1:n.*235+91C=
ENST00000522476.5:c.557+91C=	ENSP00000427894.1:n.557+91C=
ENST00000522665.5:n.78+91C=
ENST00000537882.2:c.512+91C=	ENSP00000437443.1:n.512+91C=
NM_001135242.1:c.755+91C=	NP_001128714.1:n.755+91C=
NM_001258432.1:c.557+91C=	NP_001245361.1:n.557+91C=
NM_001258433.1:c.512+91C=	NP_001245362.1:n.512+91C=
NM_006096.3:c.755+91C= , LRG_258t1:c.755+91C=	NP_006087.2:n.755+91C=
XM_011516791.1:c.806+91C=	XP_011515093.1:n.806+91C=
XM_011516792.1:c.188+91C=	XP_011515094.1:n.188+91C=
XM_011516792.2:c.188+91C=	XP_011515094.1:n.188+91C=
NM_001135242.2:c.755+91C=	NP_001128714.1:n.755+91C=
NM_001258432.2:c.557+91C=	NP_001245361.1:n.557+91C=
NM_001258433.2:c.512+91C=	NP_001245362.1:n.512+91C=
NM_001374844.1:c.806+91C=	NP_001361773.1:n.806+91C=
NM_001374845.1:c.755+91C=	NP_001361774.1:n.755+91C=
NM_001374846.1:c.755+91C=	NP_001361775.1:n.755+91C=
NM_001374847.1:c.557+91C=	NP_001361776.1:n.557+91C=
NM_006096.4:c.755+91C= MANE Select	NP_006087.2:n.755+91C=