Canonical Allele Identifier: CA1821166224

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248725_133248727delinsCTG , CM000670.2:g.133248725_133248727delinsCTG	GRCh38
NC_000008.10:g.134260968_134260970delinsCTG , CM000670.1:g.134260968_134260970delinsCTG	GRCh37
NC_000008.9:g.134330150_134330152delinsCTG	NCBI36
NG_007943.1:g.53529_53531delinsCAG , LRG_258:g.53529_53531delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.743_745delinsCAG MANE Select	ENSP00000319977.8:p.Thr248=
ENST00000537882.3:c.743_745delinsCAG	ENSP00000437443.2:p.Thr248=
ENST00000675056.1:n.73_75delinsCAG
ENST00000675068.1:c.45_47delinsCAG
ENST00000675172.1:c.339_341delinsCAG	ENSP00000502297.1:n.339_341delinsCAG
ENST00000675273.1:n.102_104delinsCAG
ENST00000675860.1:n.508_510delinsCAG
ENST00000676444.1:n.774_776delinsCAG
ENST00000323851.11:c.743_745delinsCAG	ENSP00000319977.7:p.Thr248=
ENST00000414097.6:c.743_745delinsCAG	ENSP00000404854.2:p.Thr248=
ENST00000517331.5:n.461_463delinsCAG
ENST00000517599.5:c.*349_*351delinsCAG	ENSP00000429172.1:n.*349_*351delinsCAG
ENST00000518066.5:c.37-6671_37-6669delinsCAG	ENSP00000431057.1:n.37-6671_37-6669delinsCAG
ENST00000518176.5:c.49-2064_49-2062delinsCAG	ENSP00000429007.1:n.49-2064_49-2062delinsCAG
ENST00000519278.5:n.1839_1841delinsCAG
ENST00000521414.5:n.205_207delinsCAG
ENST00000521664.1:n.493_495delinsCAG
ENST00000522377.5:c.*223_*225delinsCAG	ENSP00000429380.1:n.*223_*225delinsCAG
ENST00000522476.5:c.545_547delinsCAG	ENSP00000427894.1:p.Thr182=
ENST00000522665.5:n.66_68delinsCAG
ENST00000537882.2:c.500_502delinsCAG	ENSP00000437443.1:p.Thr167=
NM_001135242.1:c.743_745delinsCAG	NP_001128714.1:p.Thr248=
NM_001258432.1:c.545_547delinsCAG	NP_001245361.1:p.Thr182=
NM_001258433.1:c.500_502delinsCAG	NP_001245362.1:p.Thr167=
NM_006096.3:c.743_745delinsCAG , LRG_258t1:c.743_745delinsCAG	NP_006087.2:p.Thr248=
XM_011516791.1:c.794_796delinsCAG	XP_011515093.1:p.Thr265=
XM_011516792.1:c.176_178delinsCAG	XP_011515094.1:p.Thr59=
XM_011516792.2:c.176_178delinsCAG	XP_011515094.1:p.Thr59=
NM_001135242.2:c.743_745delinsCAG	NP_001128714.1:p.Thr248=
NM_001258432.2:c.545_547delinsCAG	NP_001245361.1:p.Thr182=
NM_001258433.2:c.500_502delinsCAG	NP_001245362.1:p.Thr167=
NM_001374844.1:c.794_796delinsCAG	NP_001361773.1:p.Thr265=
NM_001374845.1:c.743_745delinsCAG	NP_001361774.1:p.Thr248=
NM_001374846.1:c.743_745delinsCAG	NP_001361775.1:p.Thr248=
NM_001374847.1:c.545_547delinsCAG	NP_001361776.1:p.Thr182=
NM_006096.4:c.743_745delinsCAG MANE Select	NP_006087.2:p.Thr248=