Canonical Allele Identifier: CA4886605

Gene: NDRG1

Linked Data

• dbSNP Id: rs779765074
• ExAC: 8:134260914 G / A
• gnomAD v2: 8-134260914-G-A
• gnomAD v4: 8-133248671-G-A
• MyVariant Identifiers: chr8:g.134260914G>A (hg19) ; chr8:g.133248671G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248671G>A , CM000670.2:g.133248671G>A	GRCh38
NC_000008.10:g.134260914G>A , CM000670.1:g.134260914G>A	GRCh37
NC_000008.9:g.134330096G>A	NCBI36
NG_007943.1:g.53585C>T , LRG_258:g.53585C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000323851.13:c.755+44C>T MANE Select	ENSP00000319977.8:n.755+44C>T
ENST00000537882.3:c.755+44C>T	ENSP00000437443.2:n.755+44C>T
ENST00000675068.1:c.57+44C>T
ENST00000675860.1:n.520+44C>T
ENST00000323851.11:c.755+44C>T	ENSP00000319977.7:n.755+44C>T
ENST00000414097.6:c.755+44C>T	ENSP00000404854.2:n.755+44C>T
ENST00000517331.5:n.473+44C>T
ENST00000517599.5:c.*361+44C>T	ENSP00000429172.1:n.*361+44C>T
ENST00000518066.5:c.37-6615C>T	ENSP00000431057.1:n.37-6615C>T
ENST00000518176.5:c.49-2008C>T	ENSP00000429007.1:n.49-2008C>T
ENST00000519278.5:n.1851+44C>T
ENST00000521414.5:n.217+44C>T
ENST00000521664.1:n.505+44C>T
ENST00000522377.5:c.*235+44C>T	ENSP00000429380.1:n.*235+44C>T
ENST00000522476.5:c.557+44C>T	ENSP00000427894.1:n.557+44C>T
ENST00000522665.5:n.78+44C>T
ENST00000537882.2:c.512+44C>T	ENSP00000437443.1:n.512+44C>T
NM_001135242.1:c.755+44C>T	NP_001128714.1:n.755+44C>T
NM_001258432.1:c.557+44C>T	NP_001245361.1:n.557+44C>T
NM_001258433.1:c.512+44C>T	NP_001245362.1:n.512+44C>T
NM_006096.3:c.755+44C>T , LRG_258t1:c.755+44C>T	NP_006087.2:n.755+44C>T
XM_011516791.1:c.806+44C>T	XP_011515093.1:n.806+44C>T
XM_011516792.1:c.188+44C>T	XP_011515094.1:n.188+44C>T
XM_011516792.2:c.188+44C>T	XP_011515094.1:n.188+44C>T
NM_001135242.2:c.755+44C>T	NP_001128714.1:n.755+44C>T
NM_001258432.2:c.557+44C>T	NP_001245361.1:n.557+44C>T
NM_001258433.2:c.512+44C>T	NP_001245362.1:n.512+44C>T
NM_001374844.1:c.806+44C>T	NP_001361773.1:n.806+44C>T
NM_001374845.1:c.755+44C>T	NP_001361774.1:n.755+44C>T
NM_001374846.1:c.755+44C>T	NP_001361775.1:n.755+44C>T
NM_001374847.1:c.557+44C>T	NP_001361776.1:n.557+44C>T
NM_006096.4:c.755+44C>T MANE Select	NP_006087.2:n.755+44C>T