Canonical Allele Identifier: CA372255171

Gene: NDRG1

Linked Data

• MyVariant Identifiers: chr8:g.134260973T>G (hg19) ; chr8:g.133248730T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248730T>G , CM000670.2:g.133248730T>G	GRCh38
NC_000008.10:g.134260973T>G , CM000670.1:g.134260973T>G	GRCh37
NC_000008.9:g.134330155T>G	NCBI36
NG_007943.1:g.53526A>C , LRG_258:g.53526A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.740A>C MANE Select	ENSP00000319977.8:p.His247Pro
ENST00000537882.3:c.740A>C	ENSP00000437443.2:p.His247Pro
ENST00000675056.1:n.70A>C
ENST00000675068.1:c.42A>C
ENST00000675172.1:c.336A>C	ENSP00000502297.1:n.336A>C
ENST00000675273.1:n.99A>C
ENST00000675860.1:n.505A>C
ENST00000676444.1:n.771A>C
ENST00000323851.11:c.740A>C	ENSP00000319977.7:p.His247Pro
ENST00000414097.6:c.740A>C	ENSP00000404854.2:p.His247Pro
ENST00000517331.5:n.458A>C
ENST00000517599.5:c.*346A>C	ENSP00000429172.1:n.*346A>C
ENST00000518066.5:c.37-6674A>C	ENSP00000431057.1:n.37-6674A>C
ENST00000518176.5:c.49-2067A>C	ENSP00000429007.1:n.49-2067A>C
ENST00000519278.5:n.1836A>C
ENST00000521414.5:n.202A>C
ENST00000521664.1:n.490A>C
ENST00000522377.5:c.*220A>C	ENSP00000429380.1:n.*220A>C
ENST00000522476.5:c.542A>C	ENSP00000427894.1:p.His181Pro
ENST00000522665.5:n.63A>C
ENST00000537882.2:c.497A>C	ENSP00000437443.1:p.His166Pro
NM_001135242.1:c.740A>C	NP_001128714.1:p.His247Pro
NM_001258432.1:c.542A>C	NP_001245361.1:p.His181Pro
NM_001258433.1:c.497A>C	NP_001245362.1:p.His166Pro
NM_006096.3:c.740A>C , LRG_258t1:c.740A>C	NP_006087.2:p.His247Pro
XM_011516791.1:c.791A>C	XP_011515093.1:p.His264Pro
XM_011516792.1:c.173A>C	XP_011515094.1:p.His58Pro
XM_011516792.2:c.173A>C	XP_011515094.1:p.His58Pro
NM_001135242.2:c.740A>C	NP_001128714.1:p.His247Pro
NM_001258432.2:c.542A>C	NP_001245361.1:p.His181Pro
NM_001258433.2:c.497A>C	NP_001245362.1:p.His166Pro
NM_001374844.1:c.791A>C	NP_001361773.1:p.His264Pro
NM_001374845.1:c.740A>C	NP_001361774.1:p.His247Pro
NM_001374846.1:c.740A>C	NP_001361775.1:p.His247Pro
NM_001374847.1:c.542A>C	NP_001361776.1:p.His181Pro
NM_006096.4:c.740A>C MANE Select	NP_006087.2:p.His247Pro