Canonical Allele Identifier: CA4886779

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133259155C>G , CM000670.2:g.133259155C>G	GRCh38
NC_000008.10:g.134271398C>G , CM000670.1:g.134271398C>G	GRCh37
NC_000008.9:g.134340580C>G	NCBI36
NG_007943.1:g.43101G>C , LRG_258:g.43101G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.389+13G>C MANE Select	NP_006087.2:n.389+13G>C
ENST00000323851.13:c.389+13G>C MANE Select	ENSP00000319977.8:n.389+13G>C
NM_001135242.1:c.389+13G>C	NP_001128714.1:n.389+13G>C
NM_001135242.2:c.389+13G>C	NP_001128714.1:n.389+13G>C
NM_001258432.1:c.191+13G>C	NP_001245361.1:n.191+13G>C
NM_001258432.2:c.191+13G>C	NP_001245361.1:n.191+13G>C
NM_001258433.1:c.146+13G>C	NP_001245362.1:n.146+13G>C
NM_001258433.2:c.146+13G>C	NP_001245362.1:n.146+13G>C
NM_001374844.1:c.389+13G>C	NP_001361773.1:n.389+13G>C
NM_001374845.1:c.389+13G>C	NP_001361774.1:n.389+13G>C
NM_001374846.1:c.389+13G>C	NP_001361775.1:n.389+13G>C
NM_001374847.1:c.191+13G>C	NP_001361776.1:n.191+13G>C
NM_006096.3:c.389+13G>C , LRG_258t1:c.389+13G>C	NP_006087.2:n.389+13G>C
ENST00000323851.11:c.389+13G>C	ENSP00000319977.7:n.389+13G>C
ENST00000414097.6:c.389+13G>C	ENSP00000404854.2:n.389+13G>C
ENST00000517331.5:n.107+13G>C
ENST00000517599.5:c.283+13G>C	ENSP00000429172.1:n.283+13G>C
ENST00000517745.1:n.232G>C
ENST00000517745.2:n.374G>C
ENST00000518010.5:n.526+13G>C
ENST00000518066.5:c.37-17099G>C	ENSP00000431057.1:n.37-17099G>C
ENST00000518094.1:n.287G>C
ENST00000518176.5:c.49-12492G>C	ENSP00000429007.1:n.49-12492G>C
ENST00000518480.5:c.191+13G>C	ENSP00000428802.1:n.191+13G>C
ENST00000519228.5:c.389+13G>C	ENSP00000429994.1:n.389+13G>C
ENST00000519580.5:c.389+13G>C	ENSP00000429272.1:n.389+13G>C
ENST00000519580.6:c.389+13G>C	ENSP00000429272.1:n.389+13G>C
ENST00000520230.5:c.440+13G>C	ENSP00000428345.1:n.440+13G>C
ENST00000520943.5:c.422+13G>C	ENSP00000429840.1:n.422+13G>C
ENST00000521544.5:c.389+13G>C	ENSP00000429524.1:n.389+13G>C
ENST00000522377.5:c.389+13G>C	ENSP00000429380.1:n.389+13G>C
ENST00000522476.5:c.191+13G>C	ENSP00000427894.1:n.191+13G>C
ENST00000522890.5:c.389+13G>C	ENSP00000428384.1:n.389+13G>C
ENST00000537882.2:c.146+13G>C	ENSP00000437443.1:n.146+13G>C
ENST00000537882.3:c.389+13G>C	ENSP00000437443.2:n.389+13G>C
ENST00000676444.1:n.420+13G>C
XM_011516791.1:c.389+13G>C	XP_011515093.1:n.389+13G>C