Canonical Allele Identifier: CA372255146
Gene: NDRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133248718A>G , CM000670.2:g.133248718A>G GRCh38
NC_000008.10:g.134260961A>G , CM000670.1:g.134260961A>G GRCh37
NC_000008.9:g.134330143A>G NCBI36
NG_007943.1:g.53538T>C , LRG_258:g.53538T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.752T>C MANE Select ENSP00000319977.8:p.Leu251Pro
ENST00000537882.3:c.752T>C ENSP00000437443.2:p.Leu251Pro
ENST00000675056.1:n.82T>C
ENST00000675068.1:c.54T>C
ENST00000675172.1:c.348T>C ENSP00000502297.1:n.348T>C
ENST00000675273.1:n.111T>C
ENST00000675860.1:n.517T>C
ENST00000323851.11:c.752T>C ENSP00000319977.7:p.Leu251Pro
ENST00000414097.6:c.752T>C ENSP00000404854.2:p.Leu251Pro
ENST00000517331.5:n.470T>C
ENST00000517599.5:c.*358T>C ENSP00000429172.1:n.*358T>C
ENST00000518066.5:c.37-6662T>C ENSP00000431057.1:n.37-6662T>C
ENST00000518176.5:c.49-2055T>C ENSP00000429007.1:n.49-2055T>C
ENST00000519278.5:n.1848T>C
ENST00000521414.5:n.214T>C
ENST00000521664.1:n.502T>C
ENST00000522377.5:c.*232T>C ENSP00000429380.1:n.*232T>C
ENST00000522476.5:c.554T>C ENSP00000427894.1:p.Leu185Pro
ENST00000522665.5:n.75T>C
ENST00000537882.2:c.509T>C ENSP00000437443.1:p.Leu170Pro
NM_001135242.1:c.752T>C NP_001128714.1:p.Leu251Pro
NM_001258432.1:c.554T>C NP_001245361.1:p.Leu185Pro
NM_001258433.1:c.509T>C NP_001245362.1:p.Leu170Pro
NM_006096.3:c.752T>C , LRG_258t1:c.752T>C NP_006087.2:p.Leu251Pro
XM_011516791.1:c.803T>C XP_011515093.1:p.Leu268Pro
XM_011516792.1:c.185T>C XP_011515094.1:p.Leu62Pro
XM_011516792.2:c.185T>C XP_011515094.1:p.Leu62Pro
NM_001135242.2:c.752T>C NP_001128714.1:p.Leu251Pro
NM_001258432.2:c.554T>C NP_001245361.1:p.Leu185Pro
NM_001258433.2:c.509T>C NP_001245362.1:p.Leu170Pro
NM_001374844.1:c.803T>C NP_001361773.1:p.Leu268Pro
NM_001374845.1:c.752T>C NP_001361774.1:p.Leu251Pro
NM_001374846.1:c.752T>C NP_001361775.1:p.Leu251Pro
NM_001374847.1:c.554T>C NP_001361776.1:p.Leu185Pro
NM_006096.4:c.752T>C MANE Select NP_006087.2:p.Leu251Pro