Canonical Allele Identifier: CA1284929

Gene: NCF2 SMG7

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183573252T>C , CM000663.2:g.183573252T>C	GRCh38
NC_000001.10:g.183542387T>C , CM000663.1:g.183542387T>C	GRCh37
NC_000001.9:g.181809010T>C	NCBI36
NG_007267.1:g.22330A>G , LRG_88:g.22330A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697329.1:n.462A>G (NCF2)
ENST00000697330.1:c.542A>G (NCF2)	ENSP00000513258.1:p.Lys181Arg
ENST00000697351.1:c.501+1235A>G (NCF2)	ENSP00000513276.1:n.501+1235A>G
ENST00000367535.8:c.542A>G (NCF2) MANE Select	ENSP00000356505.4:p.Lys181Arg
ENST00000367535.7:c.542A>G (NCF2)	ENSP00000356505.3:p.Lys181Arg
ENST00000367536.5:c.542A>G (NCF2)	ENSP00000356506.1:p.Lys181Arg
ENST00000413720.5:c.407A>G (NCF2)	ENSP00000399294.1:p.Lys136Arg
ENST00000418089.5:c.367-2413A>G (NCF2)	ENSP00000407217.1:n.367-2413A>G
ENST00000495321.1:n.233+22062T>C (SMG7)
NM_000433.3:c.542A>G , LRG_88t1:c.542A>G (NCF2)	NP_000424.2:p.Lys181Arg
NM_001127651.2:c.542A>G (NCF2)	NP_001121123.1:p.Lys181Arg
NM_001190789.1:c.367-2413A>G (NCF2)	NP_001177718.1:n.367-2413A>G
NM_001190794.1:c.407A>G (NCF2)	NP_001177723.1:p.Lys136Arg
XM_005245207.1:c.501+1235A>G (NCF2)	XP_005245264.1:n.501+1235A>G
XM_011509580.1:c.542A>G (NCF2)	XP_011507882.1:p.Lys181Arg
XM_011509581.1:c.542A>G (NCF2)	XP_011507883.1:p.Lys181Arg
XR_921801.1:n.746A>G (NCF2)
NM_000433.4:c.542A>G (NCF2) MANE Select	NP_000424.2:p.Lys181Arg
NM_001127651.3:c.542A>G (NCF2)	NP_001121123.1:p.Lys181Arg
NM_001190789.2:c.367-2413A>G (NCF2)	NP_001177718.1:n.367-2413A>G
NM_001190794.2:c.407A>G (NCF2)	NP_001177723.1:p.Lys136Arg