Canonical Allele Identifier: CA2404070739
Gene: NCF4 HGNC NCBI
NCF4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36864753_36864754delinsTG , CM000684.2:g.36864753_36864754delinsTG GRCh38
NC_000022.10:g.37260795_37260796delinsTG , CM000684.1:g.37260795_37260796delinsTG GRCh37
NC_000022.9:g.35590741_35590742delinsTG NCBI36
NG_023400.1:g.8766_8767delinsTG , LRG_159:g.8766_8767delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000248899.11:c.118-166_118-165delinsTG (NCF4) MANE Select ENSP00000248899.6:n.118-166_118-165delinsTG
ENST00000397147.7:c.118-166_118-165delinsTG (NCF4) ENSP00000380334.4:n.118-166_118-165delinsTG
ENST00000650698.1:c.-192-166_-192-165delinsTG (NCF4) ENSP00000498381.1:n.-192-166_-192-165delinsTG
ENST00000650827.1:c.-192-166_-192-165delinsTG (NCF4) ENSP00000498212.1:n.-192-166_-192-165delinsTG
ENST00000651053.1:n.423-166_423-165delinsTG (NCF4)
ENST00000248899.10:c.118-166_118-165delinsTG (NCF4) ENSP00000248899.6:n.118-166_118-165delinsTG
ENST00000397147.6:c.118-166_118-165delinsTG (NCF4) ENSP00000380334.4:n.118-166_118-165delinsTG
ENST00000447071.5:c.-192-166_-192-165delinsTG (NCF4) ENSP00000414958.1:n.-192-166_-192-165delinsTG
NM_000631.4:c.118-166_118-165delinsTG (NCF4) NP_000622.2:n.118-166_118-165delinsTG
NM_013416.3:c.118-166_118-165delinsTG , LRG_159t1:c.118-166_118-165delinsTG (NCF4) NP_038202.2:n.118-166_118-165delinsTG
XM_011530198.1:c.292-166_292-165delinsTG (NCF4) XP_011528500.1:n.292-166_292-165delinsTG
XM_011530199.1:c.262-166_262-165delinsTG (NCF4) XP_011528501.1:n.262-166_262-165delinsTG
NR_147197.1:n.351+5339_351+5340delinsCA (NCF4-AS1)
XM_017028808.1:c.-192-166_-192-165delinsTG (NCF4) XP_016884297.1:n.-192-166_-192-165delinsTG
NM_000631.5:c.118-166_118-165delinsTG (NCF4) MANE Select NP_000622.2:n.118-166_118-165delinsTG
NM_013416.4:c.118-166_118-165delinsTG (NCF4) NP_038202.2:n.118-166_118-165delinsTG