Canonical Allele Identifier: CA186375958

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133254596C>T , CM000670.2:g.133254596C>T	GRCh38
NC_000008.10:g.134266839C>T , CM000670.1:g.134266839C>T	GRCh37
NC_000008.9:g.134336021C>T	NCBI36
NG_007943.1:g.47660G>A , LRG_258:g.47660G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.538-1G>A MANE Select	NP_006087.2:n.538-1G>A
ENST00000323851.13:c.538-1G>A MANE Select	ENSP00000319977.8:n.538-1G>A
NM_001135242.1:c.538-1G>A	NP_001128714.1:n.538-1G>A
NM_001135242.2:c.538-1G>A	NP_001128714.1:n.538-1G>A
NM_001258432.1:c.340-1G>A	NP_001245361.1:n.340-1G>A
NM_001258432.2:c.340-1G>A	NP_001245361.1:n.340-1G>A
NM_001258433.1:c.295-1G>A	NP_001245362.1:n.295-1G>A
NM_001258433.2:c.295-1G>A	NP_001245362.1:n.295-1G>A
NM_001374844.1:c.589-1G>A	NP_001361773.1:n.589-1G>A
NM_001374845.1:c.538-1G>A	NP_001361774.1:n.538-1G>A
NM_001374846.1:c.538-1G>A	NP_001361775.1:n.538-1G>A
NM_001374847.1:c.340-1G>A	NP_001361776.1:n.340-1G>A
NM_006096.3:c.538-1G>A , LRG_258t1:c.538-1G>A	NP_006087.2:n.538-1G>A
ENST00000323851.11:c.538-1G>A	ENSP00000319977.7:n.538-1G>A
ENST00000414097.6:c.538-1G>A	ENSP00000404854.2:n.538-1G>A
ENST00000517331.5:n.256-1G>A
ENST00000517599.5:c.*144-1G>A	ENSP00000429172.1:n.*144-1G>A
ENST00000518066.5:c.37-12540G>A	ENSP00000431057.1:n.37-12540G>A
ENST00000518176.5:c.49-7933G>A	ENSP00000429007.1:n.49-7933G>A
ENST00000519278.5:n.1633G>A
ENST00000521664.1:n.287G>A
ENST00000522377.5:c.*18-1G>A	ENSP00000429380.1:n.*18-1G>A
ENST00000522476.5:c.340-1G>A	ENSP00000427894.1:n.340-1G>A
ENST00000537882.2:c.295-1G>A	ENSP00000437443.1:n.295-1G>A
ENST00000537882.3:c.538-1G>A	ENSP00000437443.2:n.538-1G>A
ENST00000674925.1:c.139-1G>A	ENSP00000501624.1:n.139-1G>A
ENST00000676124.1:n.28-1G>A
ENST00000676222.1:c.62-1G>A
ENST00000676444.1:n.569-1G>A
XM_011516791.1:c.589-1G>A	XP_011515093.1:n.589-1G>A
XM_011516792.1:c.-30-1G>A	XP_011515094.1:n.-30-1G>A
XM_011516792.2:c.-30-1G>A	XP_011515094.1:n.-30-1G>A