Canonical Allele Identifier: CA2746921174

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183563555_183563592del , CM000663.2:g.183563555_183563592del GRCh38
NC_000001.10:g.183532690_183532727del , CM000663.1:g.183532690_183532727del GRCh37
NC_000001.9:g.181799313_181799350del NCBI36
NG_007267.1:g.31996_32033del , LRG_88:g.31996_32033del

Transcript Alleles

HGVS Amino-acid change
ENST00000469280.2:n.466_503del (NCF2)
ENST00000697329.1:n.947-1_983del (NCF2)
ENST00000697330.1:c.1027-1_1063del (NCF2)
ENST00000697351.1:c.919-1_955del (NCF2)
ENST00000367535.8:c.1027-1_1063del (NCF2)
ENST00000367535.7:c.1027-1_1063del (NCF2)
ENST00000367536.5:c.1027-1_1063del (NCF2)
ENST00000413720.5:c.892-1_928del (NCF2)
ENST00000418089.5:c.784-1_820del (NCF2)
ENST00000419402.1:c.244-1_280del (NCF2)
ENST00000420553.5:c.-21-1_16del (NCF2)
ENST00000469280.1:n.466_503del (NCF2)
ENST00000495321.1:n.233+12365_233+12402del (SMG7)
NM_000433.3:c.1027-1_1063del , LRG_88t1:c.1027-1_1063del (NCF2)
NM_001127651.2:c.1027-1_1063del (NCF2)
NM_001190789.1:c.784-1_820del (NCF2)
NM_001190794.1:c.892-1_928del (NCF2)
XM_005245207.1:c.919-1_955del (NCF2)
XM_011509580.1:c.1027-1_1063del (NCF2)
XM_011509581.1:c.1027-1_1063del (NCF2)
XR_921801.1:n.1089-1_1125del (NCF2)
NM_000433.4:c.1027-1_1063del (NCF2)
NM_001127651.3:c.1027-1_1063del (NCF2)
NM_001190789.2:c.784-1_820del (NCF2)
NM_001190794.2:c.892-1_928del (NCF2)