Canonical Allele Identifier: CA2404072282

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36867434G= , CM000684.2:g.36867434G=	GRCh38
NC_000022.10:g.37263476G= , CM000684.1:g.37263476G=	GRCh37
NC_000022.9:g.35593422G=	NCBI36
NG_023400.1:g.11447G= , LRG_159:g.11447G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000631.5:c.314G= (NCF4) MANE Select	NP_000622.2:p.Arg105=
ENST00000248899.11:c.314G= (NCF4) MANE Select	ENSP00000248899.6:p.Arg105=
NM_000631.4:c.314G= (NCF4)	NP_000622.2:p.Arg105=
NM_013416.3:c.314G= , LRG_159t1:c.314G= (NCF4)	NP_038202.2:p.Arg105=
NM_013416.4:c.314G= (NCF4)	NP_038202.2:p.Arg105=
NR_147197.1:n.351+2659C= (NCF4-AS1)
ENST00000248899.10:c.314G= (NCF4)	ENSP00000248899.6:p.Arg105=
ENST00000397147.6:c.314G= (NCF4)	ENSP00000380334.4:p.Arg105=
ENST00000397147.7:c.314G= (NCF4)	ENSP00000380334.4:p.Arg105=
ENST00000447071.5:c.5G= (NCF4)	ENSP00000414958.1:p.Arg2=
ENST00000650698.1:c.5G= (NCF4)	ENSP00000498381.1:p.Arg2=
ENST00000650827.1:c.5G= (NCF4)	ENSP00000498212.1:p.Arg2=
ENST00000651053.1:n.619G= (NCF4)
XM_011530198.1:c.488G= (NCF4)	XP_011528500.1:p.Arg163=
XM_011530199.1:c.458G= (NCF4)	XP_011528501.1:p.Arg153=
XM_017028808.1:c.5G= (NCF4)	XP_016884297.1:p.Arg2=