Canonical Allele Identifier: CA4886712

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133256759G>A , CM000670.2:g.133256759G>A	GRCh38
NC_000008.10:g.134269002G>A , CM000670.1:g.134269002G>A	GRCh37
NC_000008.9:g.134338184G>A	NCBI36
NG_007943.1:g.45497C>T , LRG_258:g.45497C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.537+18C>T MANE Select	NP_006087.2:n.537+18C>T
ENST00000323851.13:c.537+18C>T MANE Select	ENSP00000319977.8:n.537+18C>T
NM_001135242.1:c.537+18C>T	NP_001128714.1:n.537+18C>T
NM_001135242.2:c.537+18C>T	NP_001128714.1:n.537+18C>T
NM_001258432.1:c.339+18C>T	NP_001245361.1:n.339+18C>T
NM_001258432.2:c.339+18C>T	NP_001245361.1:n.339+18C>T
NM_001258433.1:c.294+18C>T	NP_001245362.1:n.294+18C>T
NM_001258433.2:c.294+18C>T	NP_001245362.1:n.294+18C>T
NM_001374844.1:c.555C>T	NP_001361773.1:p.Val185=
NM_001374845.1:c.537+18C>T	NP_001361774.1:n.537+18C>T
NM_001374846.1:c.537+18C>T	NP_001361775.1:n.537+18C>T
NM_001374847.1:c.339+18C>T	NP_001361776.1:n.339+18C>T
NM_006096.3:c.537+18C>T , LRG_258t1:c.537+18C>T	NP_006087.2:n.537+18C>T
ENST00000323851.11:c.537+18C>T	ENSP00000319977.7:n.537+18C>T
ENST00000414097.6:c.537+18C>T	ENSP00000404854.2:n.537+18C>T
ENST00000517331.5:n.255+18C>T
ENST00000517599.5:c.*143+18C>T	ENSP00000429172.1:n.*143+18C>T
ENST00000518066.5:c.37-14703C>T	ENSP00000431057.1:n.37-14703C>T
ENST00000518176.5:c.49-10096C>T	ENSP00000429007.1:n.49-10096C>T
ENST00000522377.5:c.537+18C>T	ENSP00000429380.1:n.537+18C>T
ENST00000522476.5:c.339+18C>T	ENSP00000427894.1:n.339+18C>T
ENST00000537882.2:c.294+18C>T	ENSP00000437443.1:n.294+18C>T
ENST00000537882.3:c.537+18C>T	ENSP00000437443.2:n.537+18C>T
ENST00000674925.1:c.105C>T	ENSP00000501624.1:p.Val35=
ENST00000676222.1:c.61+1607C>T
ENST00000676444.1:n.568+18C>T
XM_011516791.1:c.555C>T	XP_011515093.1:p.Val185=