Canonical Allele Identifier: CA1147798042

Gene: NCF2 SMG7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183590587C= , CM000663.2:g.183590587C=	GRCh38
NC_000001.10:g.183559722C= , CM000663.1:g.183559722C=	GRCh37
NC_000001.9:g.181826345C=	NCBI36
NG_007267.1:g.4995G= , LRG_88:g.4995G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697330.1:c.-30-228G= (NCF2)	ENSP00000513258.1:n.-30-228G=
ENST00000697352.1:n.5G= (NCF2)
ENST00000697353.1:n.83+36G= (NCF2)
ENST00000367536.5:c.-30-228G= (NCF2)	ENSP00000356506.1:n.-30-228G=
ENST00000413720.5:c.-258G= (NCF2)	ENSP00000399294.1:n.-258G=
ENST00000418089.5:c.-258G= (NCF2)	ENSP00000407217.1:n.-258G=
ENST00000495321.1:n.234-7182C= (SMG7)
NM_000433.3:c.-258G= , LRG_88t1:c.-258G= (NCF2)	NP_000424.2:n.-258G=
NM_001127651.2:c.-30-228G= (NCF2)	NP_001121123.1:n.-30-228G=
NM_001190789.1:c.-258G= (NCF2)	NP_001177718.1:n.-258G=
NM_001190794.1:c.-258G= (NCF2)	NP_001177723.1:n.-258G=
XM_011509580.1:c.-31+36G= (NCF2)	XP_011507882.1:n.-31+36G=
XM_011509581.1:c.-96G= (NCF2)	XP_011507883.1:n.-96G=
NM_001127651.3:c.-30-228G= (NCF2)	NP_001121123.1:n.-30-228G=