Canonical Allele Identifier: CA2688673153

Gene: NDRG1

Linked Data

• gnomAD v4: 8-133258318-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133258322del , CM000670.2:g.133258322del	GRCh38
NC_000008.10:g.134270565del , CM000670.1:g.134270565del	GRCh37
NC_000008.9:g.134339747del	NCBI36
NG_007943.1:g.43937del , LRG_258:g.43937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.450+47del MANE Select	ENSP00000319977.8:n.450+47del
ENST00000519580.6:c.450+47del	ENSP00000429272.1:n.450+47del
ENST00000537882.3:c.450+47del	ENSP00000437443.2:n.450+47del
ENST00000676222.1:c.61+47del
ENST00000676444.1:n.481+47del
ENST00000323851.11:c.450+47del	ENSP00000319977.7:n.450+47del
ENST00000414097.6:c.450+47del	ENSP00000404854.2:n.450+47del
ENST00000517331.5:n.168+47del
ENST00000517599.5:c.*56+47del	ENSP00000429172.1:n.*56+47del
ENST00000518010.5:n.526+849del
ENST00000518066.5:c.37-16263del	ENSP00000431057.1:n.37-16263del
ENST00000518176.5:c.49-11656del	ENSP00000429007.1:n.49-11656del
ENST00000518480.5:c.252+47del	ENSP00000428802.1:n.252+47del
ENST00000519228.5:c.450+47del	ENSP00000429994.1:n.450+47del
ENST00000519580.5:c.450+47del	ENSP00000429272.1:n.450+47del
ENST00000520230.5:c.501+47del	ENSP00000428345.1:n.501+47del
ENST00000522377.5:c.450+47del	ENSP00000429380.1:n.450+47del
ENST00000522476.5:c.252+47del	ENSP00000427894.1:n.252+47del
ENST00000522890.5:c.450+47del	ENSP00000428384.1:n.450+47del
ENST00000537882.2:c.207+47del	ENSP00000437443.1:n.207+47del
NM_001135242.1:c.450+47del	NP_001128714.1:n.450+47del
NM_001258432.1:c.252+47del	NP_001245361.1:n.252+47del
NM_001258433.1:c.207+47del	NP_001245362.1:n.207+47del
NM_006096.3:c.450+47del , LRG_258t1:c.450+47del	NP_006087.2:n.450+47del
XM_011516791.1:c.450+47del	XP_011515093.1:n.450+47del
NM_001135242.2:c.450+47del	NP_001128714.1:n.450+47del
NM_001258432.2:c.252+47del	NP_001245361.1:n.252+47del
NM_001258433.2:c.207+47del	NP_001245362.1:n.207+47del
NM_001374844.1:c.450+47del	NP_001361773.1:n.450+47del
NM_001374845.1:c.450+47del	NP_001361774.1:n.450+47del
NM_001374846.1:c.450+47del	NP_001361775.1:n.450+47del
NM_001374847.1:c.252+47del	NP_001361776.1:n.252+47del
NM_006096.4:c.450+47del MANE Select	NP_006087.2:n.450+47del