Canonical Allele Identifier: CA10588272

Gene: NCF2 SMG7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183556175T>G , CM000663.2:g.183556175T>G	GRCh38
NC_000001.10:g.183525310T>G , CM000663.1:g.183525310T>G	GRCh37
NC_000001.9:g.181791933T>G	NCBI36
NG_007267.1:g.39407A>C , LRG_88:g.39407A>C
NG_029808.1:g.88805T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469280.2:n.964A>C (NCF2)
ENST00000697329.1:n.1444A>C (NCF2)
ENST00000697330.1:c.1524A>C (NCF2)	ENSP00000513258.1:p.Lys508Asn
ENST00000697351.1:c.1416A>C (NCF2)	ENSP00000513276.1:p.Lys472Asn
ENST00000367535.8:c.1524A>C (NCF2) MANE Select	ENSP00000356505.4:p.Lys508Asn
ENST00000367535.7:c.1524A>C (NCF2)	ENSP00000356505.3:p.Lys508Asn
ENST00000367536.5:c.1524A>C (NCF2)	ENSP00000356506.1:p.Lys508Asn
ENST00000413720.5:c.1389A>C (NCF2)	ENSP00000399294.1:p.Lys463Asn
ENST00000418089.5:c.1281A>C (NCF2)	ENSP00000407217.1:p.Lys427Asn
ENST00000495321.1:n.233+4985T>G (SMG7)
NM_000433.3:c.1524A>C , LRG_88t1:c.1524A>C (NCF2)	NP_000424.2:p.Lys508Asn
NM_001127651.2:c.1524A>C (NCF2)	NP_001121123.1:p.Lys508Asn
NM_001190789.1:c.1281A>C (NCF2)	NP_001177718.1:p.Lys427Asn
NM_001190794.1:c.1389A>C (NCF2)	NP_001177723.1:p.Lys463Asn
XM_005245207.1:c.1416A>C (NCF2)	XP_005245264.1:p.Lys472Asn
XM_011509580.1:c.1524A>C (NCF2)	XP_011507882.1:p.Lys508Asn
XM_011509581.1:c.1524A>C (NCF2)	XP_011507883.1:p.Lys508Asn
NM_000433.4:c.1524A>C (NCF2) MANE Select	NP_000424.2:p.Lys508Asn
NM_001127651.3:c.1524A>C (NCF2)	NP_001121123.1:p.Lys508Asn
NM_001190789.2:c.1281A>C (NCF2)	NP_001177718.1:p.Lys427Asn
NM_001190794.2:c.1389A>C (NCF2)	NP_001177723.1:p.Lys463Asn