Canonical Allele Identifier: CA4886857

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133264553T>C , CM000670.2:g.133264553T>C	GRCh38
NC_000008.10:g.134276796T>C , CM000670.1:g.134276796T>C	GRCh37
NC_000008.9:g.134345978T>C	NCBI36
NG_007943.1:g.37703A>G , LRG_258:g.37703A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.199A>G MANE Select	ENSP00000319977.8:p.Met67Val
ENST00000517745.2:n.171A>G
ENST00000519580.6:c.199A>G	ENSP00000429272.1:p.Met67Val
ENST00000537882.3:c.199A>G	ENSP00000437443.2:p.Met67Val
ENST00000674536.1:n.181A>G
ENST00000674705.1:n.140A>G
ENST00000674902.1:c.402A>G	ENSP00000501764.1:n.402A>G
ENST00000675010.1:n.373A>G
ENST00000675357.1:c.163A>G	ENSP00000502209.1:p.Met55Val
ENST00000675531.1:n.100A>G
ENST00000675600.1:c.181A>G	ENSP00000501905.1:p.Met61Val
ENST00000676005.1:c.199A>G	ENSP00000501604.1:p.Met67Val
ENST00000676375.1:c.199A>G	ENSP00000502695.1:p.Met67Val
ENST00000676444.1:n.230A>G
ENST00000323851.11:c.199A>G	ENSP00000319977.7:p.Met67Val
ENST00000414097.6:c.199A>G	ENSP00000404854.2:p.Met67Val
ENST00000517599.5:c.100-2386A>G	ENSP00000429172.1:n.100-2386A>G
ENST00000517745.1:n.29A>G
ENST00000518010.5:n.336A>G
ENST00000518066.5:c.36+19723A>G	ENSP00000431057.1:n.36+19723A>G
ENST00000518176.5:c.49-17890A>G	ENSP00000429007.1:n.49-17890A>G
ENST00000518480.5:c.1A>G	ENSP00000428802.1:p.Met1Val
ENST00000519228.5:c.199A>G	ENSP00000429994.1:p.Met67Val
ENST00000519580.5:c.199A>G	ENSP00000429272.1:p.Met67Val
ENST00000520230.5:c.250A>G	ENSP00000428345.1:p.Met84Val
ENST00000520943.5:c.232A>G	ENSP00000429840.1:p.Met78Val
ENST00000521544.5:c.199A>G	ENSP00000429524.1:p.Met67Val
ENST00000522377.5:c.199A>G	ENSP00000429380.1:p.Met67Val
ENST00000522476.5:c.1A>G	ENSP00000427894.1:p.Met1Val
ENST00000522738.1:c.361A>G	ENSP00000428991.1:p.Met121Val
ENST00000522890.5:c.199A>G	ENSP00000428384.1:p.Met67Val
ENST00000523892.5:c.1A>G	ENSP00000430171.1:p.Met1Val
ENST00000523931.1:n.440A>G
ENST00000537882.2:c.-38-2386A>G	ENSP00000437443.1:n.-38-2386A>G
NM_001135242.1:c.199A>G	NP_001128714.1:p.Met67Val
NM_001258432.1:c.1A>G	NP_001245361.1:p.Met1Val
NM_001258433.1:c.-38-2386A>G	NP_001245362.1:n.-38-2386A>G
NM_006096.3:c.199A>G , LRG_258t1:c.199A>G	NP_006087.2:p.Met67Val
XM_011516791.1:c.199A>G	XP_011515093.1:p.Met67Val
NM_001135242.2:c.199A>G	NP_001128714.1:p.Met67Val
NM_001258432.2:c.1A>G	NP_001245361.1:p.Met1Val
NM_001258433.2:c.-38-2386A>G	NP_001245362.1:n.-38-2386A>G
NM_001374844.1:c.199A>G	NP_001361773.1:p.Met67Val
NM_001374845.1:c.199A>G	NP_001361774.1:p.Met67Val
NM_001374846.1:c.199A>G	NP_001361775.1:p.Met67Val
NM_001374847.1:c.1A>G	NP_001361776.1:p.Met1Val
NM_006096.4:c.199A>G MANE Select	NP_006087.2:p.Met67Val