Canonical Allele Identifier: CA2404070851
Gene: NCF4 HGNC NCBI
NCF4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36864955A= , CM000684.2:g.36864955A= GRCh38
NC_000022.10:g.37260997A= , CM000684.1:g.37260997A= GRCh37
NC_000022.9:g.35590943A= NCBI36
NG_023400.1:g.8968A= , LRG_159:g.8968A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248899.11:c.154A= (NCF4) MANE Select ENSP00000248899.6:p.Lys52=
ENST00000397147.7:c.154A= (NCF4) ENSP00000380334.4:p.Lys52=
ENST00000650698.1:c.-156A= (NCF4) ENSP00000498381.1:n.-156A=
ENST00000650827.1:c.-156A= (NCF4) ENSP00000498212.1:n.-156A=
ENST00000651053.1:n.459A= (NCF4)
ENST00000248899.10:c.154A= (NCF4) ENSP00000248899.6:p.Lys52=
ENST00000397147.6:c.154A= (NCF4) ENSP00000380334.4:p.Lys52=
ENST00000447071.5:c.-156A= (NCF4) ENSP00000414958.1:n.-156A=
NM_000631.4:c.154A= (NCF4) NP_000622.2:p.Lys52=
NM_013416.3:c.154A= , LRG_159t1:c.154A= (NCF4) NP_038202.2:p.Lys52=
XM_011530198.1:c.328A= (NCF4) XP_011528500.1:p.Lys110=
XM_011530199.1:c.298A= (NCF4) XP_011528501.1:p.Lys100=
NR_147197.1:n.351+5138T= (NCF4-AS1)
XM_017028808.1:c.-156A= (NCF4) XP_016884297.1:n.-156A=
NM_000631.5:c.154A= (NCF4) MANE Select NP_000622.2:p.Lys52=
NM_013416.4:c.154A= (NCF4) NP_038202.2:p.Lys52=