Canonical Allele Identifier: CA372255882

Gene: NDRG1

Linked Data

• MyVariant Identifiers: chr8:g.134270626T>A (hg19) ; chr8:g.133258383T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133258383T>A , CM000670.2:g.133258383T>A	GRCh38
NC_000008.10:g.134270626T>A , CM000670.1:g.134270626T>A	GRCh37
NC_000008.9:g.134339808T>A	NCBI36
NG_007943.1:g.43873A>T , LRG_258:g.43873A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000323851.13:c.433A>T MANE Select	ENSP00000319977.8:p.Ile145Phe
ENST00000519580.6:c.433A>T	ENSP00000429272.1:p.Ile145Phe
ENST00000537882.3:c.433A>T	ENSP00000437443.2:p.Ile145Phe
ENST00000676222.1:c.44A>T
ENST00000676444.1:n.464A>T
ENST00000323851.11:c.433A>T	ENSP00000319977.7:p.Ile145Phe
ENST00000414097.6:c.433A>T	ENSP00000404854.2:p.Ile145Phe
ENST00000517331.5:n.151A>T
ENST00000517599.5:c.*39A>T	ENSP00000429172.1:n.*39A>T
ENST00000518010.5:n.526+785A>T
ENST00000518066.5:c.37-16327A>T	ENSP00000431057.1:n.37-16327A>T
ENST00000518176.5:c.49-11720A>T	ENSP00000429007.1:n.49-11720A>T
ENST00000518480.5:c.235A>T	ENSP00000428802.1:p.Ile79Phe
ENST00000519228.5:c.433A>T	ENSP00000429994.1:p.Ile145Phe
ENST00000519580.5:c.433A>T	ENSP00000429272.1:p.Ile145Phe
ENST00000520230.5:c.484A>T	ENSP00000428345.1:p.Ile162Phe
ENST00000520943.5:c.466A>T	ENSP00000429840.1:p.Ile156Phe
ENST00000522377.5:c.433A>T	ENSP00000429380.1:p.Ile145Phe
ENST00000522476.5:c.235A>T	ENSP00000427894.1:p.Ile79Phe
ENST00000522890.5:c.433A>T	ENSP00000428384.1:p.Ile145Phe
ENST00000537882.2:c.190A>T	ENSP00000437443.1:p.Ile64Phe
NM_001135242.1:c.433A>T	NP_001128714.1:p.Ile145Phe
NM_001258432.1:c.235A>T	NP_001245361.1:p.Ile79Phe
NM_001258433.1:c.190A>T	NP_001245362.1:p.Ile64Phe
NM_006096.3:c.433A>T , LRG_258t1:c.433A>T	NP_006087.2:p.Ile145Phe
XM_011516791.1:c.433A>T	XP_011515093.1:p.Ile145Phe
NM_001135242.2:c.433A>T	NP_001128714.1:p.Ile145Phe
NM_001258432.2:c.235A>T	NP_001245361.1:p.Ile79Phe
NM_001258433.2:c.190A>T	NP_001245362.1:p.Ile64Phe
NM_001374844.1:c.433A>T	NP_001361773.1:p.Ile145Phe
NM_001374845.1:c.433A>T	NP_001361774.1:p.Ile145Phe
NM_001374846.1:c.433A>T	NP_001361775.1:p.Ile145Phe
NM_001374847.1:c.235A>T	NP_001361776.1:p.Ile79Phe
NM_006096.4:c.433A>T MANE Select	NP_006087.2:p.Ile145Phe