Canonical Allele Identifier: CA2688674259

Gene: NDRG1

Linked Data

• gnomAD v4: 8-133248897-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133248897_133248898insTC , CM000670.2:g.133248897_133248898insTC	GRCh38
NC_000008.10:g.134261140_134261141insTC , CM000670.1:g.134261140_134261141insTC	GRCh37
NC_000008.9:g.134330322_134330323insTC	NCBI36
NG_007943.1:g.53358_53359insGA , LRG_258:g.53358_53359insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323851.13:c.699-127_699-126insGA MANE Select	ENSP00000319977.8:n.699-127_699-126insGA
ENST00000537882.3:c.699-127_699-126insGA	ENSP00000437443.2:n.699-127_699-126insGA
ENST00000675056.1:n.29-127_29-126insGA
ENST00000675172.1:c.295-127_295-126insGA	ENSP00000502297.1:n.295-127_295-126insGA
ENST00000675273.1:n.58-127_58-126insGA
ENST00000675860.1:n.464-127_464-126insGA
ENST00000676444.1:n.730-127_730-126insGA
ENST00000323851.11:c.699-127_699-126insGA	ENSP00000319977.7:n.699-127_699-126insGA
ENST00000414097.6:c.699-127_699-126insGA	ENSP00000404854.2:n.699-127_699-126insGA
ENST00000517331.5:n.417-127_417-126insGA
ENST00000517599.5:c.*305-127_*305-126insGA	ENSP00000429172.1:n.*305-127_*305-126insGA
ENST00000518066.5:c.37-6842_37-6841insGA	ENSP00000431057.1:n.37-6842_37-6841insGA
ENST00000518176.5:c.49-2235_49-2234insGA	ENSP00000429007.1:n.49-2235_49-2234insGA
ENST00000519278.5:n.1795-127_1795-126insGA
ENST00000521414.5:n.161-127_161-126insGA
ENST00000521664.1:n.449-127_449-126insGA
ENST00000522377.5:c.*179-127_*179-126insGA	ENSP00000429380.1:n.*179-127_*179-126insGA
ENST00000522476.5:c.501-127_501-126insGA	ENSP00000427894.1:n.501-127_501-126insGA
ENST00000522665.5:n.22-127_22-126insGA
ENST00000537882.2:c.456-127_456-126insGA	ENSP00000437443.1:n.456-127_456-126insGA
NM_001135242.1:c.699-127_699-126insGA	NP_001128714.1:n.699-127_699-126insGA
NM_001258432.1:c.501-127_501-126insGA	NP_001245361.1:n.501-127_501-126insGA
NM_001258433.1:c.456-127_456-126insGA	NP_001245362.1:n.456-127_456-126insGA
NM_006096.3:c.699-127_699-126insGA , LRG_258t1:c.699-127_699-126insGA	NP_006087.2:n.699-127_699-126insGA
XM_011516791.1:c.750-127_750-126insGA	XP_011515093.1:n.750-127_750-126insGA
XM_011516792.1:c.132-127_132-126insGA	XP_011515094.1:n.132-127_132-126insGA
XM_011516792.2:c.132-127_132-126insGA	XP_011515094.1:n.132-127_132-126insGA
NM_001135242.2:c.699-127_699-126insGA	NP_001128714.1:n.699-127_699-126insGA
NM_001258432.2:c.501-127_501-126insGA	NP_001245361.1:n.501-127_501-126insGA
NM_001258433.2:c.456-127_456-126insGA	NP_001245362.1:n.456-127_456-126insGA
NM_001374844.1:c.750-127_750-126insGA	NP_001361773.1:n.750-127_750-126insGA
NM_001374845.1:c.699-127_699-126insGA	NP_001361774.1:n.699-127_699-126insGA
NM_001374846.1:c.699-127_699-126insGA	NP_001361775.1:n.699-127_699-126insGA
NM_001374847.1:c.501-127_501-126insGA	NP_001361776.1:n.501-127_501-126insGA
NM_006096.4:c.699-127_699-126insGA MANE Select	NP_006087.2:n.699-127_699-126insGA