Canonical Allele Identifier: CA10584286
Gene: NDRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133250457dup , CM000670.2:g.133250457dup GRCh38
NC_000008.10:g.134262700dup , CM000670.1:g.134262700dup GRCh37
NC_000008.9:g.134331882dup NCBI36
NG_007943.1:g.51799dup , LRG_258:g.51799dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.681dup MANE Select ENSP00000319977.8:p.Ile228HisfsTer13
ENST00000537882.3:c.681dup ENSP00000437443.2:p.Ile228HisfsTer13
ENST00000675172.1:c.277dup ENSP00000502297.1:n.277dup
ENST00000675273.1:n.58-1686dup
ENST00000675860.1:n.446dup
ENST00000676142.1:n.87dup
ENST00000676444.1:n.712dup
ENST00000323851.11:c.681dup ENSP00000319977.7:p.Ile228HisfsTer13
ENST00000414097.6:c.681dup ENSP00000404854.2:p.Ile228HisfsTer13
ENST00000517331.5:n.399dup
ENST00000517599.5:c.*287dup ENSP00000429172.1:n.*287dup
ENST00000518066.5:c.37-8401dup ENSP00000431057.1:n.37-8401dup
ENST00000518176.5:c.49-3794dup ENSP00000429007.1:n.49-3794dup
ENST00000519278.5:n.1777dup
ENST00000521664.1:n.431dup
ENST00000522377.5:c.*161dup ENSP00000429380.1:n.*161dup
ENST00000522476.5:c.483dup ENSP00000427894.1:p.Ile162HisfsTer13
ENST00000522665.5:n.4dup
ENST00000537882.2:c.438dup ENSP00000437443.1:p.Ile147HisfsTer13
NM_001135242.1:c.681dup NP_001128714.1:p.Ile228HisfsTer13
NM_001258432.1:c.483dup NP_001245361.1:p.Ile162HisfsTer13
NM_001258433.1:c.438dup NP_001245362.1:p.Ile147HisfsTer13
NM_006096.3:c.681dup , LRG_258t1:c.681dup NP_006087.2:p.Ile228HisfsTer13
XM_011516791.1:c.732dup XP_011515093.1:p.Ile245HisfsTer13
XM_011516792.1:c.114dup XP_011515094.1:p.Ile39HisfsTer13
XM_011516792.2:c.114dup XP_011515094.1:p.Ile39HisfsTer13
NM_001135242.2:c.681dup NP_001128714.1:p.Ile228HisfsTer13
NM_001258432.2:c.483dup NP_001245361.1:p.Ile162HisfsTer13
NM_001258433.2:c.438dup NP_001245362.1:p.Ile147HisfsTer13
NM_001374844.1:c.732dup NP_001361773.1:p.Ile245HisfsTer13
NM_001374845.1:c.681dup NP_001361774.1:p.Ile228HisfsTer13
NM_001374846.1:c.681dup NP_001361775.1:p.Ile228HisfsTer13
NM_001374847.1:c.483dup NP_001361776.1:p.Ile162HisfsTer13
NM_006096.4:c.681dup MANE Select NP_006087.2:p.Ile228HisfsTer13