Canonical Allele Identifier: CA343704587

Gene: NCF2 SMG7

Linked Data

• MyVariant Identifiers: chr1:g.183532641C>A (hg19) ; chr1:g.183563506C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183563506C>A , CM000663.2:g.183563506C>A	GRCh38
NC_000001.10:g.183532641C>A , CM000663.1:g.183532641C>A	GRCh37
NC_000001.9:g.181799264C>A	NCBI36
NG_007267.1:g.32076G>T , LRG_88:g.32076G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469280.2:n.546G>T (NCF2)
ENST00000697329.1:n.1026G>T (NCF2)
ENST00000697330.1:c.1106G>T (NCF2)	ENSP00000513258.1:p.Gly369Val
ENST00000697351.1:c.998G>T (NCF2)	ENSP00000513276.1:p.Gly333Val
ENST00000367535.8:c.1106G>T (NCF2) MANE Select	ENSP00000356505.4:p.Gly369Val
ENST00000367535.7:c.1106G>T (NCF2)	ENSP00000356505.3:p.Gly369Val
ENST00000367536.5:c.1106G>T (NCF2)	ENSP00000356506.1:p.Gly369Val
ENST00000413720.5:c.971G>T (NCF2)	ENSP00000399294.1:p.Gly324Val
ENST00000418089.5:c.863G>T (NCF2)	ENSP00000407217.1:p.Gly288Val
ENST00000419402.1:c.323G>T (NCF2)	ENSP00000406198.1:p.Gly108Val
ENST00000420553.5:c.59G>T (NCF2)	ENSP00000397228.1:p.Gly20Val
ENST00000469280.1:n.546G>T (NCF2)
ENST00000495321.1:n.233+12316C>A (SMG7)
NM_000433.3:c.1106G>T , LRG_88t1:c.1106G>T (NCF2)	NP_000424.2:p.Gly369Val
NM_001127651.2:c.1106G>T (NCF2)	NP_001121123.1:p.Gly369Val
NM_001190789.1:c.863G>T (NCF2)	NP_001177718.1:p.Gly288Val
NM_001190794.1:c.971G>T (NCF2)	NP_001177723.1:p.Gly324Val
XM_005245207.1:c.998G>T (NCF2)	XP_005245264.1:p.Gly333Val
XM_011509580.1:c.1106G>T (NCF2)	XP_011507882.1:p.Gly369Val
XM_011509581.1:c.1106G>T (NCF2)	XP_011507883.1:p.Gly369Val
XR_921801.1:n.1168G>T (NCF2)
NM_000433.4:c.1106G>T (NCF2) MANE Select	NP_000424.2:p.Gly369Val
NM_001127651.3:c.1106G>T (NCF2)	NP_001121123.1:p.Gly369Val
NM_001190789.2:c.863G>T (NCF2)	NP_001177718.1:p.Gly288Val
NM_001190794.2:c.971G>T (NCF2)	NP_001177723.1:p.Gly324Val