Canonical Allele Identifier: CA463019444
Gene: NDRG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.134260987T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133248744T>A , CM000670.2:g.133248744T>A GRCh38
NC_000008.10:g.134260987T>A , CM000670.1:g.134260987T>A GRCh37
NC_000008.9:g.134330169T>A NCBI36
NG_007943.1:g.53512A>T , LRG_258:g.53512A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.726A>T MANE Select ENSP00000319977.8:p.Pro242=
ENST00000537882.3:c.726A>T ENSP00000437443.2:p.Pro242=
ENST00000675056.1:n.56A>T
ENST00000675068.1:c.28A>T
ENST00000675172.1:c.322A>T ENSP00000502297.1:n.322A>T
ENST00000675273.1:n.85A>T
ENST00000675860.1:n.491A>T
ENST00000676444.1:n.757A>T
ENST00000323851.11:c.726A>T ENSP00000319977.7:p.Pro242=
ENST00000414097.6:c.726A>T ENSP00000404854.2:p.Pro242=
ENST00000517331.5:n.444A>T
ENST00000517599.5:c.*332A>T ENSP00000429172.1:n.*332A>T
ENST00000518066.5:c.37-6688A>T ENSP00000431057.1:n.37-6688A>T
ENST00000518176.5:c.49-2081A>T ENSP00000429007.1:n.49-2081A>T
ENST00000519278.5:n.1822A>T
ENST00000521414.5:n.188A>T
ENST00000521664.1:n.476A>T
ENST00000522377.5:c.*206A>T ENSP00000429380.1:n.*206A>T
ENST00000522476.5:c.528A>T ENSP00000427894.1:p.Pro176=
ENST00000522665.5:n.49A>T
ENST00000537882.2:c.483A>T ENSP00000437443.1:p.Pro161=
NM_001135242.1:c.726A>T NP_001128714.1:p.Pro242=
NM_001258432.1:c.528A>T NP_001245361.1:p.Pro176=
NM_001258433.1:c.483A>T NP_001245362.1:p.Pro161=
NM_006096.3:c.726A>T , LRG_258t1:c.726A>T NP_006087.2:p.Pro242=
XM_011516791.1:c.777A>T XP_011515093.1:p.Pro259=
XM_011516792.1:c.159A>T XP_011515094.1:p.Pro53=
XM_011516792.2:c.159A>T XP_011515094.1:p.Pro53=
NM_001135242.2:c.726A>T NP_001128714.1:p.Pro242=
NM_001258432.2:c.528A>T NP_001245361.1:p.Pro176=
NM_001258433.2:c.483A>T NP_001245362.1:p.Pro161=
NM_001374844.1:c.777A>T NP_001361773.1:p.Pro259=
NM_001374845.1:c.726A>T NP_001361774.1:p.Pro242=
NM_001374846.1:c.726A>T NP_001361775.1:p.Pro242=
NM_001374847.1:c.528A>T NP_001361776.1:p.Pro176=
NM_006096.4:c.726A>T MANE Select NP_006087.2:p.Pro242=