Canonical Allele Identifier: CA372254900

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133246614A>G , CM000670.2:g.133246614A>G	GRCh38
NC_000008.10:g.134258857A>G , CM000670.1:g.134258857A>G	GRCh37
NC_000008.9:g.134328039A>G	NCBI36
NG_007943.1:g.55642T>C , LRG_258:g.55642T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.855+2T>C MANE Select	NP_006087.2:n.855+2T>C
ENST00000323851.13:c.855+2T>C MANE Select	ENSP00000319977.8:n.855+2T>C
NM_001135242.1:c.855+2T>C	NP_001128714.1:n.855+2T>C
NM_001135242.2:c.855+2T>C	NP_001128714.1:n.855+2T>C
NM_001258432.1:c.657+2T>C	NP_001245361.1:n.657+2T>C
NM_001258432.2:c.657+2T>C	NP_001245361.1:n.657+2T>C
NM_001258433.1:c.612+2T>C	NP_001245362.1:n.612+2T>C
NM_001258433.2:c.612+2T>C	NP_001245362.1:n.612+2T>C
NM_001374844.1:c.906+2T>C	NP_001361773.1:n.906+2T>C
NM_001374845.1:c.855+2T>C	NP_001361774.1:n.855+2T>C
NM_001374846.1:c.855+2T>C	NP_001361775.1:n.855+2T>C
NM_001374847.1:c.657+2T>C	NP_001361776.1:n.657+2T>C
NM_006096.3:c.855+2T>C , LRG_258t1:c.855+2T>C	NP_006087.2:n.855+2T>C
ENST00000323851.11:c.855+2T>C	ENSP00000319977.7:n.855+2T>C
ENST00000414097.6:c.855+2T>C	ENSP00000404854.2:n.855+2T>C
ENST00000517331.5:n.573+2T>C
ENST00000517599.5:c.*461+2T>C	ENSP00000429172.1:n.*461+2T>C
ENST00000518066.5:c.37-4558T>C	ENSP00000431057.1:n.37-4558T>C
ENST00000518176.5:c.96+2T>C	ENSP00000429007.1:n.96+2T>C
ENST00000519278.5:n.1951+2T>C
ENST00000521414.5:n.317+2T>C
ENST00000522476.5:c.657+2T>C	ENSP00000427894.1:n.657+2T>C
ENST00000522665.5:n.178+2T>C
ENST00000537882.2:c.612+2T>C	ENSP00000437443.1:n.612+2T>C
ENST00000537882.3:c.855+2T>C	ENSP00000437443.2:n.855+2T>C
ENST00000675568.1:c.50T>C	ENSP00000501738.1:p.Val17Ala
XM_011516791.1:c.906+2T>C	XP_011515093.1:n.906+2T>C
XM_011516792.1:c.288+2T>C	XP_011515094.1:n.288+2T>C
XM_011516792.2:c.288+2T>C	XP_011515094.1:n.288+2T>C