Canonical Allele Identifier: CA463217108

Gene: NDRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133239022G>A , CM000670.2:g.133239022G>A	GRCh38
NC_000008.10:g.134251265G>A , CM000670.1:g.134251265G>A	GRCh37
NC_000008.9:g.134320447G>A	NCBI36
NG_007943.1:g.63234C>T , LRG_258:g.63234C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006096.4:c.1041C>T MANE Select	NP_006087.2:p.Ser347=
ENST00000323851.13:c.1041C>T MANE Select	ENSP00000319977.8:p.Ser347=
NM_001135242.1:c.1041C>T	NP_001128714.1:p.Ser347=
NM_001135242.2:c.1041C>T	NP_001128714.1:p.Ser347=
NM_001258432.1:c.843C>T	NP_001245361.1:p.Ser281=
NM_001258432.2:c.843C>T	NP_001245361.1:p.Ser281=
NM_001258433.1:c.798C>T	NP_001245362.1:p.Ser266=
NM_001258433.2:c.798C>T	NP_001245362.1:p.Ser266=
NM_001374844.1:c.1092C>T	NP_001361773.1:p.Ser364=
NM_001374845.1:c.1041C>T	NP_001361774.1:p.Ser347=
NM_001374846.1:c.1041C>T	NP_001361775.1:p.Ser347=
NM_001374847.1:c.843C>T	NP_001361776.1:p.Ser281=
NM_006096.3:c.1041C>T , LRG_258t1:c.1041C>T	NP_006087.2:p.Ser347=
ENST00000323851.11:c.1041C>T	ENSP00000319977.7:p.Ser347=
ENST00000414097.6:c.1041C>T	ENSP00000404854.2:p.Ser347=
ENST00000517599.5:c.*647C>T	ENSP00000429172.1:n.*647C>T
ENST00000518066.5:c.168C>T	ENSP00000431057.1:p.Ser56=
ENST00000518176.5:c.282C>T	ENSP00000429007.1:p.Ser94=
ENST00000519278.5:n.2137C>T
ENST00000521026.5:n.299C>T
ENST00000521414.5:n.503C>T
ENST00000521438.1:n.2456+50C>T
ENST00000522476.5:c.843C>T	ENSP00000427894.1:p.Ser281=
ENST00000537882.2:c.798C>T	ENSP00000437443.1:p.Ser266=
ENST00000537882.3:c.1041C>T	ENSP00000437443.2:p.Ser347=
XM_011516791.1:c.1092C>T	XP_011515093.1:p.Ser364=
XM_011516792.1:c.474C>T	XP_011515094.1:p.Ser158=
XM_011516792.2:c.474C>T	XP_011515094.1:p.Ser158=