Canonical Allele Identifier: CA1821167422
Gene: NDRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133258281_133258282delinsTG , CM000670.2:g.133258281_133258282delinsTG GRCh38
NC_000008.10:g.134270524_134270525delinsTG , CM000670.1:g.134270524_134270525delinsTG GRCh37
NC_000008.9:g.134339706_134339707delinsTG NCBI36
NG_007943.1:g.43974_43975delinsCA , LRG_258:g.43974_43975delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000323851.13:c.450+84_450+85delinsCA MANE Select ENSP00000319977.8:n.450+84_450+85delinsCA...
ENST00000519580.6:c.450+84_450+85delinsCA ENSP00000429272.1:n.450+84_450+85delinsCA...
ENST00000537882.3:c.450+84_450+85delinsCA ENSP00000437443.2:n.450+84_450+85delinsCA...
ENST00000676222.1:c.61+84_61+85delinsCA
ENST00000676444.1:n.481+84_481+85delinsCA
ENST00000323851.11:c.450+84_450+85delinsCA ENSP00000319977.7:n.450+84_450+85delinsCA...
ENST00000414097.6:c.450+84_450+85delinsCA ENSP00000404854.2:n.450+84_450+85delinsCA...
ENST00000517331.5:n.168+84_168+85delinsCA
ENST00000517599.5:c.*56+84_*56+85delinsCA ENSP00000429172.1:n.*56+84_*56+85delinsCA...
ENST00000518010.5:n.526+886_526+887delinsCA
ENST00000518066.5:c.37-16226_37-16225delinsCA ENSP00000431057.1:n.37-16226_37-16225deli...
ENST00000518176.5:c.49-11619_49-11618delinsCA ENSP00000429007.1:n.49-11619_49-11618deli...
ENST00000518480.5:c.252+84_252+85delinsCA ENSP00000428802.1:n.252+84_252+85delinsCA...
ENST00000519228.5:c.450+84_450+85delinsCA ENSP00000429994.1:n.450+84_450+85delinsCA...
ENST00000519580.5:c.450+84_450+85delinsCA ENSP00000429272.1:n.450+84_450+85delinsCA...
ENST00000520230.5:c.501+84_501+85delinsCA ENSP00000428345.1:n.501+84_501+85delinsCA...
ENST00000522377.5:c.450+84_450+85delinsCA ENSP00000429380.1:n.450+84_450+85delinsCA...
ENST00000522476.5:c.252+84_252+85delinsCA ENSP00000427894.1:n.252+84_252+85delinsCA...
ENST00000522890.5:c.450+84_450+85delinsCA ENSP00000428384.1:n.450+84_450+85delinsCA...
ENST00000537882.2:c.207+84_207+85delinsCA ENSP00000437443.1:n.207+84_207+85delinsCA...
NM_001135242.1:c.450+84_450+85delinsCA NP_001128714.1:n.450+84_450+85delinsCA
NM_001258432.1:c.252+84_252+85delinsCA NP_001245361.1:n.252+84_252+85delinsCA
NM_001258433.1:c.207+84_207+85delinsCA NP_001245362.1:n.207+84_207+85delinsCA
NM_006096.3:c.450+84_450+85delinsCA , LRG_258t1:c.450+84_450+85delinsCA NP_006087.2:n.450+84_450+85delinsCA
XM_011516791.1:c.450+84_450+85delinsCA XP_011515093.1:n.450+84_450+85delinsCA
NM_001135242.2:c.450+84_450+85delinsCA NP_001128714.1:n.450+84_450+85delinsCA
NM_001258432.2:c.252+84_252+85delinsCA NP_001245361.1:n.252+84_252+85delinsCA
NM_001258433.2:c.207+84_207+85delinsCA NP_001245362.1:n.207+84_207+85delinsCA
NM_001374844.1:c.450+84_450+85delinsCA NP_001361773.1:n.450+84_450+85delinsCA
NM_001374845.1:c.450+84_450+85delinsCA NP_001361774.1:n.450+84_450+85delinsCA
NM_001374846.1:c.450+84_450+85delinsCA NP_001361775.1:n.450+84_450+85delinsCA
NM_001374847.1:c.252+84_252+85delinsCA NP_001361776.1:n.252+84_252+85delinsCA
NM_006096.4:c.450+84_450+85delinsCA MANE Select NP_006087.2:n.450+84_450+85delinsCA