Canonical Allele Identifier: CA1821167397

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133258275_133258279delinsCCCTT , CM000670.2:g.133258275_133258279delinsCCCTT	GRCh38
NC_000008.10:g.134270518_134270522delinsCCCTT , CM000670.1:g.134270518_134270522delinsCCCTT	GRCh37
NC_000008.9:g.134339700_134339704delinsCCCTT	NCBI36
NG_007943.1:g.43977_43981delinsAAGGG , LRG_258:g.43977_43981delinsAAGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000323851.13:c.450+87_450+91delinsAAGGG MANE Select	ENSP00000319977.8:n.450+87_450+91delinsAA...
ENST00000519580.6:c.450+87_450+91delinsAAGGG	ENSP00000429272.1:n.450+87_450+91delinsAA...
ENST00000537882.3:c.450+87_450+91delinsAAGGG	ENSP00000437443.2:n.450+87_450+91delinsAA...
ENST00000676222.1:c.61+87_61+91delinsAAGGG
ENST00000676444.1:n.481+87_481+91delinsAAGGG
ENST00000323851.11:c.450+87_450+91delinsAAGGG	ENSP00000319977.7:n.450+87_450+91delinsAA...
ENST00000414097.6:c.450+87_450+91delinsAAGGG	ENSP00000404854.2:n.450+87_450+91delinsAA...
ENST00000517331.5:n.168+87_168+91delinsAAGGG
ENST00000517599.5:c.*56+87_*56+91delinsAAGGG	ENSP00000429172.1:n.*56+87_*56+91delinsAA...
ENST00000518010.5:n.526+889_526+893delinsAAGGG
ENST00000518066.5:c.37-16223_37-16219delinsAAGGG	ENSP00000431057.1:n.37-16223_37-16219deli...
ENST00000518176.5:c.49-11616_49-11612delinsAAGGG	ENSP00000429007.1:n.49-11616_49-11612deli...
ENST00000518480.5:c.252+87_252+91delinsAAGGG	ENSP00000428802.1:n.252+87_252+91delinsAA...
ENST00000519228.5:c.450+87_450+91delinsAAGGG	ENSP00000429994.1:n.450+87_450+91delinsAA...
ENST00000519580.5:c.450+87_450+91delinsAAGGG	ENSP00000429272.1:n.450+87_450+91delinsAA...
ENST00000520230.5:c.501+87_501+91delinsAAGGG	ENSP00000428345.1:n.501+87_501+91delinsAA...
ENST00000522377.5:c.450+87_450+91delinsAAGGG	ENSP00000429380.1:n.450+87_450+91delinsAA...
ENST00000522476.5:c.252+87_252+91delinsAAGGG	ENSP00000427894.1:n.252+87_252+91delinsAA...
ENST00000522890.5:c.450+87_450+91delinsAAGGG	ENSP00000428384.1:n.450+87_450+91delinsAA...
ENST00000537882.2:c.207+87_207+91delinsAAGGG	ENSP00000437443.1:n.207+87_207+91delinsAA...
NM_001135242.1:c.450+87_450+91delinsAAGGG	NP_001128714.1:n.450+87_450+91delinsAAGGG...
NM_001258432.1:c.252+87_252+91delinsAAGGG	NP_001245361.1:n.252+87_252+91delinsAAGGG...
NM_001258433.1:c.207+87_207+91delinsAAGGG	NP_001245362.1:n.207+87_207+91delinsAAGGG...
NM_006096.3:c.450+87_450+91delinsAAGGG , LRG_258t1:c.450+87_450+91delinsAAGGG	NP_006087.2:n.450+87_450+91delinsAAGGG
XM_011516791.1:c.450+87_450+91delinsAAGGG	XP_011515093.1:n.450+87_450+91delinsAAGGG...
NM_001135242.2:c.450+87_450+91delinsAAGGG	NP_001128714.1:n.450+87_450+91delinsAAGGG...
NM_001258432.2:c.252+87_252+91delinsAAGGG	NP_001245361.1:n.252+87_252+91delinsAAGGG...
NM_001258433.2:c.207+87_207+91delinsAAGGG	NP_001245362.1:n.207+87_207+91delinsAAGGG...
NM_001374844.1:c.450+87_450+91delinsAAGGG	NP_001361773.1:n.450+87_450+91delinsAAGGG...
NM_001374845.1:c.450+87_450+91delinsAAGGG	NP_001361774.1:n.450+87_450+91delinsAAGGG...
NM_001374846.1:c.450+87_450+91delinsAAGGG	NP_001361775.1:n.450+87_450+91delinsAAGGG...
NM_001374847.1:c.252+87_252+91delinsAAGGG	NP_001361776.1:n.252+87_252+91delinsAAGGG...
NM_006096.4:c.450+87_450+91delinsAAGGG MANE Select	NP_006087.2:n.450+87_450+91delinsAAGGG