Canonical Allele Identifier: CA343704454

Gene: NCF2 SMG7

Linked Data

• MyVariant Identifiers: chr1:g.183532578G>A (hg19) ; chr1:g.183563443G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183563443G>A , CM000663.2:g.183563443G>A	GRCh38
NC_000001.10:g.183532578G>A , CM000663.1:g.183532578G>A	GRCh37
NC_000001.9:g.181799201G>A	NCBI36
NG_007267.1:g.32139C>T , LRG_88:g.32139C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469280.2:n.609C>T (NCF2)
ENST00000697329.1:n.1089C>T (NCF2)
ENST00000697330.1:c.1169C>T (NCF2)	ENSP00000513258.1:p.Thr390Ile
ENST00000697351.1:c.1061C>T (NCF2)	ENSP00000513276.1:p.Thr354Ile
ENST00000367535.8:c.1169C>T (NCF2) MANE Select	ENSP00000356505.4:p.Thr390Ile
ENST00000367535.7:c.1169C>T (NCF2)	ENSP00000356505.3:p.Thr390Ile
ENST00000367536.5:c.1169C>T (NCF2)	ENSP00000356506.1:p.Thr390Ile
ENST00000413720.5:c.1034C>T (NCF2)	ENSP00000399294.1:p.Thr345Ile
ENST00000418089.5:c.926C>T (NCF2)	ENSP00000407217.1:p.Thr309Ile
ENST00000419402.1:c.386C>T (NCF2)	ENSP00000406198.1:p.Thr129Ile
ENST00000420553.5:c.122C>T (NCF2)	ENSP00000397228.1:p.Thr41Ile
ENST00000469280.1:n.609C>T (NCF2)
ENST00000495321.1:n.233+12253G>A (SMG7)
NM_000433.3:c.1169C>T , LRG_88t1:c.1169C>T (NCF2)	NP_000424.2:p.Thr390Ile
NM_001127651.2:c.1169C>T (NCF2)	NP_001121123.1:p.Thr390Ile
NM_001190789.1:c.926C>T (NCF2)	NP_001177718.1:p.Thr309Ile
NM_001190794.1:c.1034C>T (NCF2)	NP_001177723.1:p.Thr345Ile
XM_005245207.1:c.1061C>T (NCF2)	XP_005245264.1:p.Thr354Ile
XM_011509580.1:c.1169C>T (NCF2)	XP_011507882.1:p.Thr390Ile
XM_011509581.1:c.1169C>T (NCF2)	XP_011507883.1:p.Thr390Ile
XR_921801.1:n.1231C>T (NCF2)
NM_000433.4:c.1169C>T (NCF2) MANE Select	NP_000424.2:p.Thr390Ile
NM_001127651.3:c.1169C>T (NCF2)	NP_001121123.1:p.Thr390Ile
NM_001190789.2:c.926C>T (NCF2)	NP_001177718.1:p.Thr309Ile
NM_001190794.2:c.1034C>T (NCF2)	NP_001177723.1:p.Thr345Ile