Canonical Allele Identifier: CA372255890
Gene: NDRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133258386A>T , CM000670.2:g.133258386A>T GRCh38
NC_000008.10:g.134270629A>T , CM000670.1:g.134270629A>T GRCh37
NC_000008.9:g.134339811A>T NCBI36
NG_007943.1:g.43870T>A , LRG_258:g.43870T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323851.13:c.430T>A MANE Select ENSP00000319977.8:p.Tyr144Asn
ENST00000519580.6:c.430T>A ENSP00000429272.1:p.Tyr144Asn
ENST00000537882.3:c.430T>A ENSP00000437443.2:p.Tyr144Asn
ENST00000676222.1:c.41T>A
ENST00000676444.1:n.461T>A
ENST00000323851.11:c.430T>A ENSP00000319977.7:p.Tyr144Asn
ENST00000414097.6:c.430T>A ENSP00000404854.2:p.Tyr144Asn
ENST00000517331.5:n.148T>A
ENST00000517599.5:c.*36T>A ENSP00000429172.1:n.*36T>A
ENST00000518010.5:n.526+782T>A
ENST00000518066.5:c.37-16330T>A ENSP00000431057.1:n.37-16330T>A
ENST00000518176.5:c.49-11723T>A ENSP00000429007.1:n.49-11723T>A
ENST00000518480.5:c.232T>A ENSP00000428802.1:p.Tyr78Asn
ENST00000519228.5:c.430T>A ENSP00000429994.1:p.Tyr144Asn
ENST00000519580.5:c.430T>A ENSP00000429272.1:p.Tyr144Asn
ENST00000520230.5:c.481T>A ENSP00000428345.1:p.Tyr161Asn
ENST00000520943.5:c.463T>A ENSP00000429840.1:p.Tyr155Asn
ENST00000522377.5:c.430T>A ENSP00000429380.1:p.Tyr144Asn
ENST00000522476.5:c.232T>A ENSP00000427894.1:p.Tyr78Asn
ENST00000522890.5:c.430T>A ENSP00000428384.1:p.Tyr144Asn
ENST00000537882.2:c.187T>A ENSP00000437443.1:p.Tyr63Asn
NM_001135242.1:c.430T>A NP_001128714.1:p.Tyr144Asn
NM_001258432.1:c.232T>A NP_001245361.1:p.Tyr78Asn
NM_001258433.1:c.187T>A NP_001245362.1:p.Tyr63Asn
NM_006096.3:c.430T>A , LRG_258t1:c.430T>A NP_006087.2:p.Tyr144Asn
XM_011516791.1:c.430T>A XP_011515093.1:p.Tyr144Asn
NM_001135242.2:c.430T>A NP_001128714.1:p.Tyr144Asn
NM_001258432.2:c.232T>A NP_001245361.1:p.Tyr78Asn
NM_001258433.2:c.187T>A NP_001245362.1:p.Tyr63Asn
NM_001374844.1:c.430T>A NP_001361773.1:p.Tyr144Asn
NM_001374845.1:c.430T>A NP_001361774.1:p.Tyr144Asn
NM_001374846.1:c.430T>A NP_001361775.1:p.Tyr144Asn
NM_001374847.1:c.232T>A NP_001361776.1:p.Tyr78Asn
NM_006096.4:c.430T>A MANE Select NP_006087.2:p.Tyr144Asn