Canonical Allele Identifier: CA372255200

Gene: NDRG1

Linked Data

• MyVariant Identifiers: chr8:g.134260988G>A (hg19) ; chr8:g.133248745G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248745G>A , CM000670.2:g.133248745G>A	GRCh38
NC_000008.10:g.134260988G>A , CM000670.1:g.134260988G>A	GRCh37
NC_000008.9:g.134330170G>A	NCBI36
NG_007943.1:g.53511C>T , LRG_258:g.53511C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.725C>T MANE Select	ENSP00000319977.8:p.Pro242Leu
ENST00000537882.3:c.725C>T	ENSP00000437443.2:p.Pro242Leu
ENST00000675056.1:n.55C>T
ENST00000675068.1:c.27C>T
ENST00000675172.1:c.321C>T	ENSP00000502297.1:n.321C>T
ENST00000675273.1:n.84C>T
ENST00000675860.1:n.490C>T
ENST00000676444.1:n.756C>T
ENST00000323851.11:c.725C>T	ENSP00000319977.7:p.Pro242Leu
ENST00000414097.6:c.725C>T	ENSP00000404854.2:p.Pro242Leu
ENST00000517331.5:n.443C>T
ENST00000517599.5:c.*331C>T	ENSP00000429172.1:n.*331C>T
ENST00000518066.5:c.37-6689C>T	ENSP00000431057.1:n.37-6689C>T
ENST00000518176.5:c.49-2082C>T	ENSP00000429007.1:n.49-2082C>T
ENST00000519278.5:n.1821C>T
ENST00000521414.5:n.187C>T
ENST00000521664.1:n.475C>T
ENST00000522377.5:c.*205C>T	ENSP00000429380.1:n.*205C>T
ENST00000522476.5:c.527C>T	ENSP00000427894.1:p.Pro176Leu
ENST00000522665.5:n.48C>T
ENST00000537882.2:c.482C>T	ENSP00000437443.1:p.Pro161Leu
NM_001135242.1:c.725C>T	NP_001128714.1:p.Pro242Leu
NM_001258432.1:c.527C>T	NP_001245361.1:p.Pro176Leu
NM_001258433.1:c.482C>T	NP_001245362.1:p.Pro161Leu
NM_006096.3:c.725C>T , LRG_258t1:c.725C>T	NP_006087.2:p.Pro242Leu
XM_011516791.1:c.776C>T	XP_011515093.1:p.Pro259Leu
XM_011516792.1:c.158C>T	XP_011515094.1:p.Pro53Leu
XM_011516792.2:c.158C>T	XP_011515094.1:p.Pro53Leu
NM_001135242.2:c.725C>T	NP_001128714.1:p.Pro242Leu
NM_001258432.2:c.527C>T	NP_001245361.1:p.Pro176Leu
NM_001258433.2:c.482C>T	NP_001245362.1:p.Pro161Leu
NM_001374844.1:c.776C>T	NP_001361773.1:p.Pro259Leu
NM_001374845.1:c.725C>T	NP_001361774.1:p.Pro242Leu
NM_001374846.1:c.725C>T	NP_001361775.1:p.Pro242Leu
NM_001374847.1:c.527C>T	NP_001361776.1:p.Pro176Leu
NM_006096.4:c.725C>T MANE Select	NP_006087.2:p.Pro242Leu