Canonical Allele Identifier: CA372256334

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133262136G>C , CM000670.2:g.133262136G>C	GRCh38
NC_000008.10:g.134274379G>C , CM000670.1:g.134274379G>C	GRCh37
NC_000008.9:g.134343561G>C	NCBI36
NG_007943.1:g.40120C>G , LRG_258:g.40120C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.237C>G MANE Select	NP_006087.2:p.Tyr79Ter
ENST00000323851.13:c.237C>G MANE Select	ENSP00000319977.8:p.Tyr79Ter
NM_001135242.1:c.237C>G	NP_001128714.1:p.Tyr79Ter
NM_001135242.2:c.237C>G	NP_001128714.1:p.Tyr79Ter
NM_001258432.1:c.39C>G	NP_001245361.1:p.Tyr13Ter
NM_001258432.2:c.39C>G	NP_001245361.1:p.Tyr13Ter
NM_001258433.1:c.-7C>G	NP_001245362.1:n.-7C>G
NM_001258433.2:c.-7C>G	NP_001245362.1:n.-7C>G
NM_001374844.1:c.237C>G	NP_001361773.1:p.Tyr79Ter
NM_001374845.1:c.237C>G	NP_001361774.1:p.Tyr79Ter
NM_001374846.1:c.237C>G	NP_001361775.1:p.Tyr79Ter
NM_001374847.1:c.39C>G	NP_001361776.1:p.Tyr13Ter
NM_006096.3:c.237C>G , LRG_258t1:c.237C>G	NP_006087.2:p.Tyr79Ter
ENST00000323851.11:c.237C>G	ENSP00000319977.7:p.Tyr79Ter
ENST00000414097.6:c.237C>G	ENSP00000404854.2:p.Tyr79Ter
ENST00000517599.5:c.131C>G	ENSP00000429172.1:p.Thr44Arg
ENST00000517745.1:n.67C>G
ENST00000517745.2:n.209C>G
ENST00000518010.5:n.374C>G
ENST00000518066.5:c.37-20080C>G	ENSP00000431057.1:n.37-20080C>G
ENST00000518094.1:n.122C>G
ENST00000518176.5:c.49-15473C>G	ENSP00000429007.1:n.49-15473C>G
ENST00000518480.5:c.39C>G	ENSP00000428802.1:p.Tyr13Ter
ENST00000519228.5:c.237C>G	ENSP00000429994.1:p.Tyr79Ter
ENST00000519580.5:c.237C>G	ENSP00000429272.1:p.Tyr79Ter
ENST00000519580.6:c.237C>G	ENSP00000429272.1:p.Tyr79Ter
ENST00000520230.5:c.288C>G	ENSP00000428345.1:p.Tyr96Ter
ENST00000520943.5:c.270C>G	ENSP00000429840.1:p.Tyr90Ter
ENST00000521544.5:c.237C>G	ENSP00000429524.1:p.Tyr79Ter
ENST00000522377.5:c.237C>G	ENSP00000429380.1:p.Tyr79Ter
ENST00000522476.5:c.39C>G	ENSP00000427894.1:p.Tyr13Ter
ENST00000522738.1:c.399C>G	ENSP00000428991.1:p.Tyr133Ter
ENST00000522890.5:c.237C>G	ENSP00000428384.1:p.Tyr79Ter
ENST00000523892.5:c.39C>G	ENSP00000430171.1:p.Tyr13Ter
ENST00000523931.1:n.478C>G
ENST00000537882.2:c.-7C>G	ENSP00000437443.1:n.-7C>G
ENST00000537882.3:c.237C>G	ENSP00000437443.2:p.Tyr79Ter
ENST00000675010.1:n.411C>G
ENST00000675429.1:n.32C>G
ENST00000675437.1:n.32C>G
ENST00000675531.1:n.187C>G
ENST00000676005.1:c.237C>G	ENSP00000501604.1:p.Tyr79Ter
ENST00000676375.1:c.237C>G	ENSP00000502695.1:p.Tyr79Ter
ENST00000676444.1:n.268C>G
XM_011516791.1:c.237C>G	XP_011515093.1:p.Tyr79Ter