Canonical Allele Identifier: CA1211968167

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183590594G= , CM000663.2:g.183590594G= GRCh38
NC_000001.10:g.183559729G= , CM000663.1:g.183559729G= GRCh37
NC_000001.9:g.181826352G= NCBI36
NG_007267.1:g.4988C= , LRG_88:g.4988C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697330.1:c.-30-235C= (NCF2) ENSP00000513258.1:n.-30-235C=
ENST00000697353.1:n.83+29C= (NCF2)
ENST00000367536.5:c.-30-235C= (NCF2) ENSP00000356506.1:n.-30-235C=
ENST00000413720.5:c.-265C= (NCF2) ENSP00000399294.1:n.-265C=
ENST00000418089.5:c.-265C= (NCF2) ENSP00000407217.1:n.-265C=
ENST00000495321.1:n.234-7175G= (SMG7)
NM_000433.3:c.-265C= , LRG_88t1:c.-265C= (NCF2) NP_000424.2:n.-265C=
NM_001127651.2:c.-30-235C= (NCF2) NP_001121123.1:n.-30-235C=
NM_001190789.1:c.-265C= (NCF2) NP_001177718.1:n.-265C=
NM_001190794.1:c.-265C= (NCF2) NP_001177723.1:n.-265C=
XM_011509580.1:c.-31+29C= (NCF2) XP_011507882.1:n.-31+29C=
NM_001127651.3:c.-30-235C= (NCF2) NP_001121123.1:n.-30-235C=