Canonical Allele Identifier: CA4886828
Gene: NDRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133262067G>A , CM000670.2:g.133262067G>A GRCh38
NC_000008.10:g.134274310G>A , CM000670.1:g.134274310G>A GRCh37
NC_000008.9:g.134343492G>A NCBI36
NG_007943.1:g.40189C>T , LRG_258:g.40189C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.306C>T MANE Select ENSP00000319977.8:p.Gly102=
ENST00000517745.2:n.278C>T
ENST00000519580.6:c.306C>T ENSP00000429272.1:p.Gly102=
ENST00000537882.3:c.306C>T ENSP00000437443.2:p.Gly102=
ENST00000675010.1:n.480C>T
ENST00000675429.1:n.101C>T
ENST00000675437.1:n.101C>T
ENST00000675531.1:n.256C>T
ENST00000676005.1:c.306C>T ENSP00000501604.1:p.Gly102=
ENST00000676444.1:n.337C>T
ENST00000323851.11:c.306C>T ENSP00000319977.7:p.Gly102=
ENST00000414097.6:c.306C>T ENSP00000404854.2:p.Gly102=
ENST00000517599.5:c.200C>T ENSP00000429172.1:p.Ala67Val
ENST00000517745.1:n.136C>T
ENST00000518010.5:n.443C>T
ENST00000518066.5:c.37-20011C>T ENSP00000431057.1:n.37-20011C>T
ENST00000518094.1:n.191C>T
ENST00000518176.5:c.49-15404C>T ENSP00000429007.1:n.49-15404C>T
ENST00000518480.5:c.108C>T ENSP00000428802.1:p.Gly36=
ENST00000519228.5:c.306C>T ENSP00000429994.1:p.Gly102=
ENST00000519580.5:c.306C>T ENSP00000429272.1:p.Gly102=
ENST00000520230.5:c.357C>T ENSP00000428345.1:p.Gly119=
ENST00000520943.5:c.339C>T ENSP00000429840.1:p.Gly113=
ENST00000521544.5:c.306C>T ENSP00000429524.1:p.Gly102=
ENST00000522377.5:c.306C>T ENSP00000429380.1:p.Gly102=
ENST00000522476.5:c.108C>T ENSP00000427894.1:p.Gly36=
ENST00000522738.1:c.468C>T ENSP00000428991.1:p.Gly156=
ENST00000522890.5:c.306C>T ENSP00000428384.1:p.Gly102=
ENST00000523892.5:c.108C>T ENSP00000430171.1:p.Gly36=
ENST00000523931.1:n.547C>T
ENST00000537882.2:c.63C>T ENSP00000437443.1:p.Gly21=
NM_001135242.1:c.306C>T NP_001128714.1:p.Gly102=
NM_001258432.1:c.108C>T NP_001245361.1:p.Gly36=
NM_001258433.1:c.63C>T NP_001245362.1:p.Gly21=
NM_006096.3:c.306C>T , LRG_258t1:c.306C>T NP_006087.2:p.Gly102=
XM_011516791.1:c.306C>T XP_011515093.1:p.Gly102=
NM_001135242.2:c.306C>T NP_001128714.1:p.Gly102=
NM_001258432.2:c.108C>T NP_001245361.1:p.Gly36=
NM_001258433.2:c.63C>T NP_001245362.1:p.Gly21=
NM_001374844.1:c.306C>T NP_001361773.1:p.Gly102=
NM_001374845.1:c.306C>T NP_001361774.1:p.Gly102=
NM_001374846.1:c.306C>T NP_001361775.1:p.Gly102=
NM_001374847.1:c.108C>T NP_001361776.1:p.Gly36=
NM_006096.4:c.306C>T MANE Select NP_006087.2:p.Gly102=