Canonical Allele Identifier: CA4886437

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133239010T>G , CM000670.2:g.133239010T>G	GRCh38
NC_000008.10:g.134251253T>G , CM000670.1:g.134251253T>G	GRCh37
NC_000008.9:g.134320435T>G	NCBI36
NG_007943.1:g.63246A>C , LRG_258:g.63246A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.1053A>C MANE Select	NP_006087.2:p.Arg351=
ENST00000323851.13:c.1053A>C MANE Select	ENSP00000319977.8:p.Arg351=
NM_001135242.1:c.1053A>C	NP_001128714.1:p.Arg351=
NM_001135242.2:c.1053A>C	NP_001128714.1:p.Arg351=
NM_001258432.1:c.855A>C	NP_001245361.1:p.Arg285=
NM_001258432.2:c.855A>C	NP_001245361.1:p.Arg285=
NM_001258433.1:c.810A>C	NP_001245362.1:p.Arg270=
NM_001258433.2:c.810A>C	NP_001245362.1:p.Arg270=
NM_001374844.1:c.1104A>C	NP_001361773.1:p.Arg368=
NM_001374845.1:c.1053A>C	NP_001361774.1:p.Arg351=
NM_001374846.1:c.1053A>C	NP_001361775.1:p.Arg351=
NM_001374847.1:c.855A>C	NP_001361776.1:p.Arg285=
NM_006096.3:c.1053A>C , LRG_258t1:c.1053A>C	NP_006087.2:p.Arg351=
ENST00000323851.11:c.1053A>C	ENSP00000319977.7:p.Arg351=
ENST00000414097.6:c.1053A>C	ENSP00000404854.2:p.Arg351=
ENST00000517599.5:c.*659A>C	ENSP00000429172.1:n.*659A>C
ENST00000518066.5:c.180A>C	ENSP00000431057.1:p.Arg60=
ENST00000518176.5:c.294A>C	ENSP00000429007.1:p.Arg98=
ENST00000519278.5:n.2149A>C
ENST00000521026.5:n.311A>C
ENST00000521414.5:n.515A>C
ENST00000521438.1:n.2456+62A>C
ENST00000522476.5:c.855A>C	ENSP00000427894.1:p.Arg285=
ENST00000537882.2:c.810A>C	ENSP00000437443.1:p.Arg270=
ENST00000537882.3:c.1053A>C	ENSP00000437443.2:p.Arg351=
XM_011516791.1:c.1104A>C	XP_011515093.1:p.Arg368=
XM_011516792.1:c.486A>C	XP_011515094.1:p.Arg162=
XM_011516792.2:c.486A>C	XP_011515094.1:p.Arg162=