Canonical Allele Identifier: CA343703658

Gene: NCF2 SMG7

Linked Data

• MyVariant Identifiers: chr1:g.183529302A>T (hg19) ; chr1:g.183560167A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183560167A>T , CM000663.2:g.183560167A>T	GRCh38
NC_000001.10:g.183529302A>T , CM000663.1:g.183529302A>T	GRCh37
NC_000001.9:g.181795925A>T	NCBI36
NG_007267.1:g.35415T>A , LRG_88:g.35415T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469280.2:n.837T>A (NCF2)
ENST00000697329.1:n.1317T>A (NCF2)
ENST00000697330.1:c.1397T>A (NCF2)	ENSP00000513258.1:p.Phe466Tyr
ENST00000697351.1:c.1289T>A (NCF2)	ENSP00000513276.1:p.Phe430Tyr
ENST00000367535.8:c.1397T>A (NCF2) MANE Select	ENSP00000356505.4:p.Phe466Tyr
ENST00000367535.7:c.1397T>A (NCF2)	ENSP00000356505.3:p.Phe466Tyr
ENST00000367536.5:c.1397T>A (NCF2)	ENSP00000356506.1:p.Phe466Tyr
ENST00000413720.5:c.1262T>A (NCF2)	ENSP00000399294.1:p.Phe421Tyr
ENST00000418089.5:c.1154T>A (NCF2)	ENSP00000407217.1:p.Phe385Tyr
ENST00000495321.1:n.233+8977A>T (SMG7)
NM_000433.3:c.1397T>A , LRG_88t1:c.1397T>A (NCF2)	NP_000424.2:p.Phe466Tyr
NM_001127651.2:c.1397T>A (NCF2)	NP_001121123.1:p.Phe466Tyr
NM_001190789.1:c.1154T>A (NCF2)	NP_001177718.1:p.Phe385Tyr
NM_001190794.1:c.1262T>A (NCF2)	NP_001177723.1:p.Phe421Tyr
XM_005245207.1:c.1289T>A (NCF2)	XP_005245264.1:p.Phe430Tyr
XM_011509580.1:c.1397T>A (NCF2)	XP_011507882.1:p.Phe466Tyr
XM_011509581.1:c.1397T>A (NCF2)	XP_011507883.1:p.Phe466Tyr
NM_000433.4:c.1397T>A (NCF2) MANE Select	NP_000424.2:p.Phe466Tyr
NM_001127651.3:c.1397T>A (NCF2)	NP_001121123.1:p.Phe466Tyr
NM_001190789.2:c.1154T>A (NCF2)	NP_001177718.1:p.Phe385Tyr
NM_001190794.2:c.1262T>A (NCF2)	NP_001177723.1:p.Phe421Tyr