Canonical Allele Identifier: CA463217393

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133239112C>T , CM000670.2:g.133239112C>T	GRCh38
NC_000008.10:g.134251355C>T , CM000670.1:g.134251355C>T	GRCh37
NC_000008.9:g.134320537C>T	NCBI36
NG_007943.1:g.63144G>A , LRG_258:g.63144G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.951G>A MANE Select	NP_006087.2:p.Ser317=
ENST00000323851.13:c.951G>A MANE Select	ENSP00000319977.8:p.Ser317=
NM_001135242.1:c.951G>A	NP_001128714.1:p.Ser317=
NM_001135242.2:c.951G>A	NP_001128714.1:p.Ser317=
NM_001258432.1:c.753G>A	NP_001245361.1:p.Ser251=
NM_001258432.2:c.753G>A	NP_001245361.1:p.Ser251=
NM_001258433.1:c.708G>A	NP_001245362.1:p.Ser236=
NM_001258433.2:c.708G>A	NP_001245362.1:p.Ser236=
NM_001374844.1:c.1002G>A	NP_001361773.1:p.Ser334=
NM_001374845.1:c.951G>A	NP_001361774.1:p.Ser317=
NM_001374846.1:c.951G>A	NP_001361775.1:p.Ser317=
NM_001374847.1:c.753G>A	NP_001361776.1:p.Ser251=
NM_006096.3:c.951G>A , LRG_258t1:c.951G>A	NP_006087.2:p.Ser317=
ENST00000323851.11:c.951G>A	ENSP00000319977.7:p.Ser317=
ENST00000414097.6:c.951G>A	ENSP00000404854.2:p.Ser317=
ENST00000517599.5:c.*557G>A	ENSP00000429172.1:n.*557G>A
ENST00000518066.5:c.78G>A	ENSP00000431057.1:p.Ser26=
ENST00000518176.5:c.192G>A	ENSP00000429007.1:p.Ser64=
ENST00000519278.5:n.2047G>A
ENST00000521026.5:n.209G>A
ENST00000521414.5:n.413G>A
ENST00000521438.1:n.2416G>A
ENST00000522476.5:c.753G>A	ENSP00000427894.1:p.Ser251=
ENST00000537882.2:c.708G>A	ENSP00000437443.1:p.Ser236=
ENST00000537882.3:c.951G>A	ENSP00000437443.2:p.Ser317=
XM_011516791.1:c.1002G>A	XP_011515093.1:p.Ser334=
XM_011516792.1:c.384G>A	XP_011515094.1:p.Ser128=
XM_011516792.2:c.384G>A	XP_011515094.1:p.Ser128=