Canonical Allele Identifier: CA372255159

Gene: NDRG1

Linked Data

• MyVariant Identifiers: chr8:g.134260968C>A (hg19) ; chr8:g.133248725C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248725C>A , CM000670.2:g.133248725C>A	GRCh38
NC_000008.10:g.134260968C>A , CM000670.1:g.134260968C>A	GRCh37
NC_000008.9:g.134330150C>A	NCBI36
NG_007943.1:g.53531G>T , LRG_258:g.53531G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.745G>T MANE Select	ENSP00000319977.8:p.Val249Phe
ENST00000537882.3:c.745G>T	ENSP00000437443.2:p.Val249Phe
ENST00000675056.1:n.75G>T
ENST00000675068.1:c.47G>T
ENST00000675172.1:c.341G>T	ENSP00000502297.1:n.341G>T
ENST00000675273.1:n.104G>T
ENST00000675860.1:n.510G>T
ENST00000676444.1:n.776G>T
ENST00000323851.11:c.745G>T	ENSP00000319977.7:p.Val249Phe
ENST00000414097.6:c.745G>T	ENSP00000404854.2:p.Val249Phe
ENST00000517331.5:n.463G>T
ENST00000517599.5:c.*351G>T	ENSP00000429172.1:n.*351G>T
ENST00000518066.5:c.37-6669G>T	ENSP00000431057.1:n.37-6669G>T
ENST00000518176.5:c.49-2062G>T	ENSP00000429007.1:n.49-2062G>T
ENST00000519278.5:n.1841G>T
ENST00000521414.5:n.207G>T
ENST00000521664.1:n.495G>T
ENST00000522377.5:c.*225G>T	ENSP00000429380.1:n.*225G>T
ENST00000522476.5:c.547G>T	ENSP00000427894.1:p.Val183Phe
ENST00000522665.5:n.68G>T
ENST00000537882.2:c.502G>T	ENSP00000437443.1:p.Val168Phe
NM_001135242.1:c.745G>T	NP_001128714.1:p.Val249Phe
NM_001258432.1:c.547G>T	NP_001245361.1:p.Val183Phe
NM_001258433.1:c.502G>T	NP_001245362.1:p.Val168Phe
NM_006096.3:c.745G>T , LRG_258t1:c.745G>T	NP_006087.2:p.Val249Phe
XM_011516791.1:c.796G>T	XP_011515093.1:p.Val266Phe
XM_011516792.1:c.178G>T	XP_011515094.1:p.Val60Phe
XM_011516792.2:c.178G>T	XP_011515094.1:p.Val60Phe
NM_001135242.2:c.745G>T	NP_001128714.1:p.Val249Phe
NM_001258432.2:c.547G>T	NP_001245361.1:p.Val183Phe
NM_001258433.2:c.502G>T	NP_001245362.1:p.Val168Phe
NM_001374844.1:c.796G>T	NP_001361773.1:p.Val266Phe
NM_001374845.1:c.745G>T	NP_001361774.1:p.Val249Phe
NM_001374846.1:c.745G>T	NP_001361775.1:p.Val249Phe
NM_001374847.1:c.547G>T	NP_001361776.1:p.Val183Phe
NM_006096.4:c.745G>T MANE Select	NP_006087.2:p.Val249Phe