Canonical Allele Identifier: CA1119428384

Gene: NDRG1

Linked Data

• dbSNP Id: rs1856464560
• gnomAD v3: 8-133257908-TACACAATTGCTCGGTGAGGATACAA-T
• gnomAD v4: 8-133257908-TACACAATTGCTCGGTGAGGATACAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133257910_133257934del , CM000670.2:g.133257910_133257934del	GRCh38
NC_000008.10:g.134270153_134270177del , CM000670.1:g.134270153_134270177del	GRCh37
NC_000008.9:g.134339335_134339359del	NCBI36
NG_007943.1:g.44323_44347del , LRG_258:g.44323_44347del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.450+433_450+457del MANE Select	ENSP00000319977.8:n.450+433_450+457del
ENST00000519580.6:c.450+433_450+457del	ENSP00000429272.1:n.450+433_450+457del
ENST00000537882.3:c.450+433_450+457del	ENSP00000437443.2:n.450+433_450+457del
ENST00000676222.1:c.61+433_61+457del
ENST00000676444.1:n.481+433_481+457del
ENST00000323851.11:c.450+433_450+457del	ENSP00000319977.7:n.450+433_450+457del
ENST00000414097.6:c.450+433_450+457del	ENSP00000404854.2:n.450+433_450+457del
ENST00000517331.5:n.168+433_168+457del
ENST00000517599.5:c.*56+433_*56+457del	ENSP00000429172.1:n.*56+433_*56+457del
ENST00000518010.5:n.527-1070_527-1046del
ENST00000518066.5:c.37-15877_37-15853del	ENSP00000431057.1:n.37-15877_37-15853del
ENST00000518176.5:c.49-11270_49-11246del	ENSP00000429007.1:n.49-11270_49-11246del
ENST00000518480.5:c.252+433_252+457del	ENSP00000428802.1:n.252+433_252+457del
ENST00000519228.5:c.450+433_450+457del	ENSP00000429994.1:n.450+433_450+457del
ENST00000519580.5:c.450+433_450+457del	ENSP00000429272.1:n.450+433_450+457del
ENST00000520230.5:c.501+433_501+457del	ENSP00000428345.1:n.501+433_501+457del
ENST00000522377.5:c.450+433_450+457del	ENSP00000429380.1:n.450+433_450+457del
ENST00000522476.5:c.252+433_252+457del	ENSP00000427894.1:n.252+433_252+457del
ENST00000522890.5:c.450+433_450+457del	ENSP00000428384.1:n.450+433_450+457del
ENST00000537882.2:c.207+433_207+457del	ENSP00000437443.1:n.207+433_207+457del
NM_001135242.1:c.450+433_450+457del	NP_001128714.1:n.450+433_450+457del
NM_001258432.1:c.252+433_252+457del	NP_001245361.1:n.252+433_252+457del
NM_001258433.1:c.207+433_207+457del	NP_001245362.1:n.207+433_207+457del
NM_006096.3:c.450+433_450+457del , LRG_258t1:c.450+433_450+457del	NP_006087.2:n.450+433_450+457del
XM_011516791.1:c.450+433_450+457del	XP_011515093.1:n.450+433_450+457del
NM_001135242.2:c.450+433_450+457del	NP_001128714.1:n.450+433_450+457del
NM_001258432.2:c.252+433_252+457del	NP_001245361.1:n.252+433_252+457del
NM_001258433.2:c.207+433_207+457del	NP_001245362.1:n.207+433_207+457del
NM_001374844.1:c.450+433_450+457del	NP_001361773.1:n.450+433_450+457del
NM_001374845.1:c.450+433_450+457del	NP_001361774.1:n.450+433_450+457del
NM_001374846.1:c.450+433_450+457del	NP_001361775.1:n.450+433_450+457del
NM_001374847.1:c.252+433_252+457del	NP_001361776.1:n.252+433_252+457del
NM_006096.4:c.450+433_450+457del MANE Select	NP_006087.2:n.450+433_450+457del