Canonical Allele Identifier: CA463019430

Gene: NDRG1

Linked Data

• MyVariant Identifiers: chr8:g.134260966G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248723G>A , CM000670.2:g.133248723G>A	GRCh38
NC_000008.10:g.134260966G>A , CM000670.1:g.134260966G>A	GRCh37
NC_000008.9:g.134330148G>A	NCBI36
NG_007943.1:g.53533C>T , LRG_258:g.53533C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.747C>T MANE Select	ENSP00000319977.8:p.Val249=
ENST00000537882.3:c.747C>T	ENSP00000437443.2:p.Val249=
ENST00000675056.1:n.77C>T
ENST00000675068.1:c.49C>T
ENST00000675172.1:c.343C>T	ENSP00000502297.1:n.343C>T
ENST00000675273.1:n.106C>T
ENST00000675860.1:n.512C>T
ENST00000323851.11:c.747C>T	ENSP00000319977.7:p.Val249=
ENST00000414097.6:c.747C>T	ENSP00000404854.2:p.Val249=
ENST00000517331.5:n.465C>T
ENST00000517599.5:c.*353C>T	ENSP00000429172.1:n.*353C>T
ENST00000518066.5:c.37-6667C>T	ENSP00000431057.1:n.37-6667C>T
ENST00000518176.5:c.49-2060C>T	ENSP00000429007.1:n.49-2060C>T
ENST00000519278.5:n.1843C>T
ENST00000521414.5:n.209C>T
ENST00000521664.1:n.497C>T
ENST00000522377.5:c.*227C>T	ENSP00000429380.1:n.*227C>T
ENST00000522476.5:c.549C>T	ENSP00000427894.1:p.Val183=
ENST00000522665.5:n.70C>T
ENST00000537882.2:c.504C>T	ENSP00000437443.1:p.Val168=
NM_001135242.1:c.747C>T	NP_001128714.1:p.Val249=
NM_001258432.1:c.549C>T	NP_001245361.1:p.Val183=
NM_001258433.1:c.504C>T	NP_001245362.1:p.Val168=
NM_006096.3:c.747C>T , LRG_258t1:c.747C>T	NP_006087.2:p.Val249=
XM_011516791.1:c.798C>T	XP_011515093.1:p.Val266=
XM_011516792.1:c.180C>T	XP_011515094.1:p.Val60=
XM_011516792.2:c.180C>T	XP_011515094.1:p.Val60=
NM_001135242.2:c.747C>T	NP_001128714.1:p.Val249=
NM_001258432.2:c.549C>T	NP_001245361.1:p.Val183=
NM_001258433.2:c.504C>T	NP_001245362.1:p.Val168=
NM_001374844.1:c.798C>T	NP_001361773.1:p.Val266=
NM_001374845.1:c.747C>T	NP_001361774.1:p.Val249=
NM_001374846.1:c.747C>T	NP_001361775.1:p.Val249=
NM_001374847.1:c.549C>T	NP_001361776.1:p.Val183=
NM_006096.4:c.747C>T MANE Select	NP_006087.2:p.Val249=