Canonical Allele Identifier: CA463020798

Gene: NDRG1

Linked Data

• ClinVar Variation Id: 2779238
• ClinVar RCV Id: RCV003745656
• MyVariant Identifiers: chr8:g.134270630G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133258387G>A , CM000670.2:g.133258387G>A	GRCh38
NC_000008.10:g.134270630G>A , CM000670.1:g.134270630G>A	GRCh37
NC_000008.9:g.134339812G>A	NCBI36
NG_007943.1:g.43869C>T , LRG_258:g.43869C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000323851.13:c.429C>T MANE Select	ENSP00000319977.8:p.Ala143=
ENST00000519580.6:c.429C>T	ENSP00000429272.1:p.Ala143=
ENST00000537882.3:c.429C>T	ENSP00000437443.2:p.Ala143=
ENST00000676222.1:c.40C>T
ENST00000676444.1:n.460C>T
ENST00000323851.11:c.429C>T	ENSP00000319977.7:p.Ala143=
ENST00000414097.6:c.429C>T	ENSP00000404854.2:p.Ala143=
ENST00000517331.5:n.147C>T
ENST00000517599.5:c.*35C>T	ENSP00000429172.1:n.*35C>T
ENST00000518010.5:n.526+781C>T
ENST00000518066.5:c.37-16331C>T	ENSP00000431057.1:n.37-16331C>T
ENST00000518176.5:c.49-11724C>T	ENSP00000429007.1:n.49-11724C>T
ENST00000518480.5:c.231C>T	ENSP00000428802.1:p.Ala77=
ENST00000519228.5:c.429C>T	ENSP00000429994.1:p.Ala143=
ENST00000519580.5:c.429C>T	ENSP00000429272.1:p.Ala143=
ENST00000520230.5:c.480C>T	ENSP00000428345.1:p.Ala160=
ENST00000520943.5:c.462C>T	ENSP00000429840.1:p.Ala154=
ENST00000522377.5:c.429C>T	ENSP00000429380.1:p.Ala143=
ENST00000522476.5:c.231C>T	ENSP00000427894.1:p.Ala77=
ENST00000522890.5:c.429C>T	ENSP00000428384.1:p.Ala143=
ENST00000537882.2:c.186C>T	ENSP00000437443.1:p.Ala62=
NM_001135242.1:c.429C>T	NP_001128714.1:p.Ala143=
NM_001258432.1:c.231C>T	NP_001245361.1:p.Ala77=
NM_001258433.1:c.186C>T	NP_001245362.1:p.Ala62=
NM_006096.3:c.429C>T , LRG_258t1:c.429C>T	NP_006087.2:p.Ala143=
XM_011516791.1:c.429C>T	XP_011515093.1:p.Ala143=
NM_001135242.2:c.429C>T	NP_001128714.1:p.Ala143=
NM_001258432.2:c.231C>T	NP_001245361.1:p.Ala77=
NM_001258433.2:c.186C>T	NP_001245362.1:p.Ala62=
NM_001374844.1:c.429C>T	NP_001361773.1:p.Ala143=
NM_001374845.1:c.429C>T	NP_001361774.1:p.Ala143=
NM_001374846.1:c.429C>T	NP_001361775.1:p.Ala143=
NM_001374847.1:c.231C>T	NP_001361776.1:p.Ala77=
NM_006096.4:c.429C>T MANE Select	NP_006087.2:p.Ala143=