Canonical Allele Identifier: CA2573620109

Gene: NCF2 SMG7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183573100A>G , CM000663.2:g.183573100A>G	GRCh38
NC_000001.10:g.183542235A>G , CM000663.1:g.183542235A>G	GRCh37
NC_000001.9:g.181808858A>G	NCBI36
NG_007267.1:g.22482T>C , LRG_88:g.22482T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697329.1:n.529+85T>C (NCF2)
ENST00000697330.1:c.609+85T>C (NCF2)	ENSP00000513258.1:n.609+85T>C
ENST00000697351.1:c.501+1387T>C (NCF2)	ENSP00000513276.1:n.501+1387T>C
ENST00000367535.8:c.609+85T>C (NCF2) MANE Select	ENSP00000356505.4:n.609+85T>C
ENST00000367535.7:c.609+85T>C (NCF2)	ENSP00000356505.3:n.609+85T>C
ENST00000367536.5:c.609+85T>C (NCF2)	ENSP00000356506.1:n.609+85T>C
ENST00000413720.5:c.474+85T>C (NCF2)	ENSP00000399294.1:n.474+85T>C
ENST00000418089.5:c.367-2261T>C (NCF2)	ENSP00000407217.1:n.367-2261T>C
ENST00000495321.1:n.233+21910A>G (SMG7)
NM_000433.3:c.609+85T>C , LRG_88t1:c.609+85T>C (NCF2)	NP_000424.2:n.609+85T>C
NM_001127651.2:c.609+85T>C (NCF2)	NP_001121123.1:n.609+85T>C
NM_001190789.1:c.367-2261T>C (NCF2)	NP_001177718.1:n.367-2261T>C
NM_001190794.1:c.474+85T>C (NCF2)	NP_001177723.1:n.474+85T>C
XM_005245207.1:c.501+1387T>C (NCF2)	XP_005245264.1:n.501+1387T>C
XM_011509580.1:c.609+85T>C (NCF2)	XP_011507882.1:n.609+85T>C
XM_011509581.1:c.609+85T>C (NCF2)	XP_011507883.1:n.609+85T>C
XR_921801.1:n.813+85T>C (NCF2)
NM_000433.4:c.609+85T>C (NCF2) MANE Select	NP_000424.2:n.609+85T>C
NM_001127651.3:c.609+85T>C (NCF2)	NP_001121123.1:n.609+85T>C
NM_001190789.2:c.367-2261T>C (NCF2)	NP_001177718.1:n.367-2261T>C
NM_001190794.2:c.474+85T>C (NCF2)	NP_001177723.1:n.474+85T>C