Canonical Allele Identifier: CA1211968012

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183590184A= , CM000663.2:g.183590184A= GRCh38
NC_000001.10:g.183559319A= , CM000663.1:g.183559319A= GRCh37
NC_000001.9:g.181825942A= NCBI36
NG_007267.1:g.5398T= , LRG_88:g.5398T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697330.1:c.146T= (NCF2) ENSP00000513258.1:p.Ile49=
ENST00000697351.1:c.146T= (NCF2) ENSP00000513276.1:p.Ile49=
ENST00000697352.1:n.246T= (NCF2)
ENST00000697353.1:n.259T= (NCF2)
ENST00000367535.8:c.146T= (NCF2) MANE Select ENSP00000356505.4:p.Ile49=
ENST00000367535.7:c.146T= (NCF2) ENSP00000356505.3:p.Ile49=
ENST00000367536.5:c.146T= (NCF2) ENSP00000356506.1:p.Ile49=
ENST00000413720.5:c.146T= (NCF2) ENSP00000399294.1:p.Ile49=
ENST00000418089.5:c.146T= (NCF2) ENSP00000407217.1:p.Ile49=
ENST00000495321.1:n.234-7585A= (SMG7)
NM_000433.3:c.146T= , LRG_88t1:c.146T= (NCF2) NP_000424.2:p.Ile49=
NM_001127651.2:c.146T= (NCF2) NP_001121123.1:p.Ile49=
NM_001190789.1:c.146T= (NCF2) NP_001177718.1:p.Ile49=
NM_001190794.1:c.146T= (NCF2) NP_001177723.1:p.Ile49=
XM_005245207.1:c.146T= (NCF2) XP_005245264.1:p.Ile49=
XM_011509580.1:c.146T= (NCF2) XP_011507882.1:p.Ile49=
XM_011509581.1:c.146T= (NCF2) XP_011507883.1:p.Ile49=
XR_921801.1:n.350T= (NCF2)
NM_000433.4:c.146T= (NCF2) MANE Select NP_000424.2:p.Ile49=
NM_001127651.3:c.146T= (NCF2) NP_001121123.1:p.Ile49=
NM_001190789.2:c.146T= (NCF2) NP_001177718.1:p.Ile49=
NM_001190794.2:c.146T= (NCF2) NP_001177723.1:p.Ile49=