Canonical Allele Identifier: CA4886490

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133242079G>A , CM000670.2:g.133242079G>A	GRCh38
NC_000008.10:g.134254322G>A , CM000670.1:g.134254322G>A	GRCh37
NC_000008.9:g.134323504G>A	NCBI36
NG_007943.1:g.60177C>T , LRG_258:g.60177C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.892-5C>T MANE Select	ENSP00000319977.8:n.892-5C>T
ENST00000537882.3:c.892-5C>T	ENSP00000437443.2:n.892-5C>T
ENST00000323851.11:c.892-5C>T	ENSP00000319977.7:n.892-5C>T
ENST00000414097.6:c.892-5C>T	ENSP00000404854.2:n.892-5C>T
ENST00000517599.5:c.*498-5C>T	ENSP00000429172.1:n.*498-5C>T
ENST00000518066.5:c.37-23C>T	ENSP00000431057.1:n.37-23C>T
ENST00000518176.5:c.133-5C>T	ENSP00000429007.1:n.133-5C>T
ENST00000519278.5:n.1988-5C>T
ENST00000521026.5:n.150-5C>T
ENST00000521414.5:n.354-5C>T
ENST00000522476.5:c.694-5C>T	ENSP00000427894.1:n.694-5C>T
ENST00000522665.5:n.215-5C>T
ENST00000523642.1:n.307-5C>T
ENST00000537882.2:c.649-5C>T	ENSP00000437443.1:n.649-5C>T
NM_001135242.1:c.892-5C>T	NP_001128714.1:n.892-5C>T
NM_001258432.1:c.694-5C>T	NP_001245361.1:n.694-5C>T
NM_001258433.1:c.649-5C>T	NP_001245362.1:n.649-5C>T
NM_006096.3:c.892-5C>T , LRG_258t1:c.892-5C>T	NP_006087.2:n.892-5C>T
XM_011516791.1:c.943-5C>T	XP_011515093.1:n.943-5C>T
XM_011516792.1:c.325-5C>T	XP_011515094.1:n.325-5C>T
XM_011516792.2:c.325-5C>T	XP_011515094.1:n.325-5C>T
NM_001135242.2:c.892-5C>T	NP_001128714.1:n.892-5C>T
NM_001258432.2:c.694-5C>T	NP_001245361.1:n.694-5C>T
NM_001258433.2:c.649-5C>T	NP_001245362.1:n.649-5C>T
NM_001374844.1:c.943-5C>T	NP_001361773.1:n.943-5C>T
NM_001374845.1:c.892-5C>T	NP_001361774.1:n.892-5C>T
NM_001374846.1:c.892-5C>T	NP_001361775.1:n.892-5C>T
NM_001374847.1:c.694-5C>T	NP_001361776.1:n.694-5C>T
NM_006096.4:c.892-5C>T MANE Select	NP_006087.2:n.892-5C>T