Canonical Allele Identifier: CA2404070857
Gene: NCF4 HGNC NCBI
NCF4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36864965_36864974delinsTCTACCGCCG , CM000684.2:g.36864965_36864974delinsTCTACCGCCG GRCh38
NC_000022.10:g.37261007_37261016delinsTCTACCGCCG , CM000684.1:g.37261007_37261016delinsTCTACCGCCG GRCh37
NC_000022.9:g.35590953_35590962delinsTCTACCGCCG NCBI36
NG_023400.1:g.8978_8987delinsTCTACCGCCG , LRG_159:g.8978_8987delinsTCTACCGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000248899.11:c.164_173delinsTCTACCGCCG (NCF4) MANE Select ENSP00000248899.6:p.Ile55=
ENST00000397147.7:c.164_173delinsTCTACCGCCG (NCF4) ENSP00000380334.4:p.Ile55=
ENST00000650698.1:c.-146_-137delinsTCTACCGCCG (NCF4) ENSP00000498381.1:n.-146_-137delinsTCTACCGCCG
ENST00000650827.1:c.-146_-137delinsTCTACCGCCG (NCF4) ENSP00000498212.1:n.-146_-137delinsTCTACCGCCG
ENST00000651053.1:n.469_478delinsTCTACCGCCG (NCF4)
ENST00000248899.10:c.164_173delinsTCTACCGCCG (NCF4) ENSP00000248899.6:p.Ile55=
ENST00000397147.6:c.164_173delinsTCTACCGCCG (NCF4) ENSP00000380334.4:p.Ile55=
ENST00000447071.5:c.-146_-137delinsTCTACCGCCG (NCF4) ENSP00000414958.1:n.-146_-137delinsTCTACCGCCG
NM_000631.4:c.164_173delinsTCTACCGCCG (NCF4) NP_000622.2:p.Ile55=
NM_013416.3:c.164_173delinsTCTACCGCCG , LRG_159t1:c.164_173delinsTCTACCGCCG (NCF4) NP_038202.2:p.Ile55=
XM_011530198.1:c.338_347delinsTCTACCGCCG (NCF4) XP_011528500.1:p.Ile113=
XM_011530199.1:c.308_317delinsTCTACCGCCG (NCF4) XP_011528501.1:p.Ile103=
NR_147197.1:n.351+5119_351+5128delinsCGGCGGTAGA (NCF4-AS1)
XM_017028808.1:c.-146_-137delinsTCTACCGCCG (NCF4) XP_016884297.1:n.-146_-137delinsTCTACCGCCG
NM_000631.5:c.164_173delinsTCTACCGCCG (NCF4) MANE Select NP_000622.2:p.Ile55=
NM_013416.4:c.164_173delinsTCTACCGCCG (NCF4) NP_038202.2:p.Ile55=