Canonical Allele Identifier: CA372255674

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133256789C>T , CM000670.2:g.133256789C>T	GRCh38
NC_000008.10:g.134269032C>T , CM000670.1:g.134269032C>T	GRCh37
NC_000008.9:g.134338214C>T	NCBI36
NG_007943.1:g.45467G>A , LRG_258:g.45467G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.525G>A MANE Select	NP_006087.2:p.Trp175Ter
ENST00000323851.13:c.525G>A MANE Select	ENSP00000319977.8:p.Trp175Ter
NM_001135242.1:c.525G>A	NP_001128714.1:p.Trp175Ter
NM_001135242.2:c.525G>A	NP_001128714.1:p.Trp175Ter
NM_001258432.1:c.327G>A	NP_001245361.1:p.Trp109Ter
NM_001258432.2:c.327G>A	NP_001245361.1:p.Trp109Ter
NM_001258433.1:c.282G>A	NP_001245362.1:p.Trp94Ter
NM_001258433.2:c.282G>A	NP_001245362.1:p.Trp94Ter
NM_001374844.1:c.525G>A	NP_001361773.1:p.Trp175Ter
NM_001374845.1:c.525G>A	NP_001361774.1:p.Trp175Ter
NM_001374846.1:c.525G>A	NP_001361775.1:p.Trp175Ter
NM_001374847.1:c.327G>A	NP_001361776.1:p.Trp109Ter
NM_006096.3:c.525G>A , LRG_258t1:c.525G>A	NP_006087.2:p.Trp175Ter
ENST00000323851.11:c.525G>A	ENSP00000319977.7:p.Trp175Ter
ENST00000414097.6:c.525G>A	ENSP00000404854.2:p.Trp175Ter
ENST00000517331.5:n.243G>A
ENST00000517599.5:c.*131G>A	ENSP00000429172.1:n.*131G>A
ENST00000518066.5:c.37-14733G>A	ENSP00000431057.1:n.37-14733G>A
ENST00000518176.5:c.49-10126G>A	ENSP00000429007.1:n.49-10126G>A
ENST00000520230.5:c.576G>A	ENSP00000428345.1:p.Trp192Ter
ENST00000522377.5:c.525G>A	ENSP00000429380.1:p.Trp175Ter
ENST00000522476.5:c.327G>A	ENSP00000427894.1:p.Trp109Ter
ENST00000537882.2:c.282G>A	ENSP00000437443.1:p.Trp94Ter
ENST00000537882.3:c.525G>A	ENSP00000437443.2:p.Trp175Ter
ENST00000674925.1:c.75G>A	ENSP00000501624.1:p.Trp25Ter
ENST00000676222.1:c.61+1577G>A
ENST00000676444.1:n.556G>A
XM_011516791.1:c.525G>A	XP_011515093.1:p.Trp175Ter