Canonical Allele Identifier: CA2404070841

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36864931G= , CM000684.2:g.36864931G=	GRCh38
NC_000022.10:g.37260973G= , CM000684.1:g.37260973G=	GRCh37
NC_000022.9:g.35590919G=	NCBI36
NG_023400.1:g.8944G= , LRG_159:g.8944G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.130G= (NCF4) MANE Select	ENSP00000248899.6:p.Glu44=
ENST00000397147.7:c.130G= (NCF4)	ENSP00000380334.4:p.Glu44=
ENST00000650698.1:c.-180G= (NCF4)	ENSP00000498381.1:n.-180G=
ENST00000650827.1:c.-180G= (NCF4)	ENSP00000498212.1:n.-180G=
ENST00000651053.1:n.435G= (NCF4)
ENST00000248899.10:c.130G= (NCF4)	ENSP00000248899.6:p.Glu44=
ENST00000397147.6:c.130G= (NCF4)	ENSP00000380334.4:p.Glu44=
ENST00000447071.5:c.-180G= (NCF4)	ENSP00000414958.1:n.-180G=
NM_000631.4:c.130G= (NCF4)	NP_000622.2:p.Glu44=
NM_013416.3:c.130G= , LRG_159t1:c.130G= (NCF4)	NP_038202.2:p.Glu44=
XM_011530198.1:c.304G= (NCF4)	XP_011528500.1:p.Glu102=
XM_011530199.1:c.274G= (NCF4)	XP_011528501.1:p.Glu92=
NR_147197.1:n.351+5162C= (NCF4-AS1)
XM_017028808.1:c.-180G= (NCF4)	XP_016884297.1:n.-180G=
NM_000631.5:c.130G= (NCF4) MANE Select	NP_000622.2:p.Glu44=
NM_013416.4:c.130G= (NCF4)	NP_038202.2:p.Glu44=