Canonical Allele Identifier: CA372254809

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133244353A>G , CM000670.2:g.133244353A>G	GRCh38
NC_000008.10:g.134256596A>G , CM000670.1:g.134256596A>G	GRCh37
NC_000008.9:g.134325778A>G	NCBI36
NG_007943.1:g.57903T>C , LRG_258:g.57903T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.891+2T>C MANE Select	NP_006087.2:n.891+2T>C
ENST00000323851.13:c.891+2T>C MANE Select	ENSP00000319977.8:n.891+2T>C
NM_001135242.1:c.891+2T>C	NP_001128714.1:n.891+2T>C
NM_001135242.2:c.891+2T>C	NP_001128714.1:n.891+2T>C
NM_001258432.1:c.693+2T>C	NP_001245361.1:n.693+2T>C
NM_001258432.2:c.693+2T>C	NP_001245361.1:n.693+2T>C
NM_001258433.1:c.648+2T>C	NP_001245362.1:n.648+2T>C
NM_001258433.2:c.648+2T>C	NP_001245362.1:n.648+2T>C
NM_001374844.1:c.942+2T>C	NP_001361773.1:n.942+2T>C
NM_001374845.1:c.891+2T>C	NP_001361774.1:n.891+2T>C
NM_001374846.1:c.891+2T>C	NP_001361775.1:n.891+2T>C
NM_001374847.1:c.693+2T>C	NP_001361776.1:n.693+2T>C
NM_006096.3:c.891+2T>C , LRG_258t1:c.891+2T>C	NP_006087.2:n.891+2T>C
ENST00000323851.11:c.891+2T>C	ENSP00000319977.7:n.891+2T>C
ENST00000414097.6:c.891+2T>C	ENSP00000404854.2:n.891+2T>C
ENST00000517599.5:c.*497+2T>C	ENSP00000429172.1:n.*497+2T>C
ENST00000518066.5:c.37-2297T>C	ENSP00000431057.1:n.37-2297T>C
ENST00000518176.5:c.132+2T>C	ENSP00000429007.1:n.132+2T>C
ENST00000519278.5:n.1987+2T>C
ENST00000521026.5:n.149+2T>C
ENST00000521414.5:n.353+2T>C
ENST00000522476.5:c.693+2T>C	ENSP00000427894.1:n.693+2T>C
ENST00000522665.5:n.214+2T>C
ENST00000523642.1:n.306+2T>C
ENST00000537882.2:c.648+2T>C	ENSP00000437443.1:n.648+2T>C
ENST00000537882.3:c.891+2T>C	ENSP00000437443.2:n.891+2T>C
ENST00000675414.1:n.36+2T>C
XM_011516791.1:c.942+2T>C	XP_011515093.1:n.942+2T>C
XM_011516792.1:c.324+2T>C	XP_011515094.1:n.324+2T>C
XM_011516792.2:c.324+2T>C	XP_011515094.1:n.324+2T>C