Canonical Allele Identifier: CA2688673008

Gene: NDRG1

Linked Data

• gnomAD v4: 8-133258244-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133258245_133258246del , CM000670.2:g.133258245_133258246del	GRCh38
NC_000008.10:g.134270488_134270489del , CM000670.1:g.134270488_134270489del	GRCh37
NC_000008.9:g.134339670_134339671del	NCBI36
NG_007943.1:g.44010_44011del , LRG_258:g.44010_44011del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.450+120_450+121del MANE Select	ENSP00000319977.8:n.450+120_450+121del
ENST00000519580.6:c.450+120_450+121del	ENSP00000429272.1:n.450+120_450+121del
ENST00000537882.3:c.450+120_450+121del	ENSP00000437443.2:n.450+120_450+121del
ENST00000676222.1:c.61+120_61+121del
ENST00000676444.1:n.481+120_481+121del
ENST00000323851.11:c.450+120_450+121del	ENSP00000319977.7:n.450+120_450+121del
ENST00000414097.6:c.450+120_450+121del	ENSP00000404854.2:n.450+120_450+121del
ENST00000517331.5:n.168+120_168+121del
ENST00000517599.5:c.*56+120_*56+121del	ENSP00000429172.1:n.*56+120_*56+121del
ENST00000518010.5:n.526+922_526+923del
ENST00000518066.5:c.37-16190_37-16189del	ENSP00000431057.1:n.37-16190_37-16189del
ENST00000518176.5:c.49-11583_49-11582del	ENSP00000429007.1:n.49-11583_49-11582del
ENST00000518480.5:c.252+120_252+121del	ENSP00000428802.1:n.252+120_252+121del
ENST00000519228.5:c.450+120_450+121del	ENSP00000429994.1:n.450+120_450+121del
ENST00000519580.5:c.450+120_450+121del	ENSP00000429272.1:n.450+120_450+121del
ENST00000520230.5:c.501+120_501+121del	ENSP00000428345.1:n.501+120_501+121del
ENST00000522377.5:c.450+120_450+121del	ENSP00000429380.1:n.450+120_450+121del
ENST00000522476.5:c.252+120_252+121del	ENSP00000427894.1:n.252+120_252+121del
ENST00000522890.5:c.450+120_450+121del	ENSP00000428384.1:n.450+120_450+121del
ENST00000537882.2:c.207+120_207+121del	ENSP00000437443.1:n.207+120_207+121del
NM_001135242.1:c.450+120_450+121del	NP_001128714.1:n.450+120_450+121del
NM_001258432.1:c.252+120_252+121del	NP_001245361.1:n.252+120_252+121del
NM_001258433.1:c.207+120_207+121del	NP_001245362.1:n.207+120_207+121del
NM_006096.3:c.450+120_450+121del , LRG_258t1:c.450+120_450+121del	NP_006087.2:n.450+120_450+121del
XM_011516791.1:c.450+120_450+121del	XP_011515093.1:n.450+120_450+121del
NM_001135242.2:c.450+120_450+121del	NP_001128714.1:n.450+120_450+121del
NM_001258432.2:c.252+120_252+121del	NP_001245361.1:n.252+120_252+121del
NM_001258433.2:c.207+120_207+121del	NP_001245362.1:n.207+120_207+121del
NM_001374844.1:c.450+120_450+121del	NP_001361773.1:n.450+120_450+121del
NM_001374845.1:c.450+120_450+121del	NP_001361774.1:n.450+120_450+121del
NM_001374846.1:c.450+120_450+121del	NP_001361775.1:n.450+120_450+121del
NM_001374847.1:c.252+120_252+121del	NP_001361776.1:n.252+120_252+121del
NM_006096.4:c.450+120_450+121del MANE Select	NP_006087.2:n.450+120_450+121del