Canonical Allele Identifier: CA2404070985

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36865204G= , CM000684.2:g.36865204G=	GRCh38
NC_000022.10:g.37261246G= , CM000684.1:g.37261246G=	GRCh37
NC_000022.9:g.35591192G=	NCBI36
NG_023400.1:g.9217G= , LRG_159:g.9217G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.271+132G= (NCF4) MANE Select	ENSP00000248899.6:n.271+132G=
ENST00000397147.7:c.271+132G= (NCF4)	ENSP00000380334.4:n.271+132G=
ENST00000650698.1:c.-39+132G= (NCF4)	ENSP00000498381.1:n.-39+132G=
ENST00000650827.1:c.-39+132G= (NCF4)	ENSP00000498212.1:n.-39+132G=
ENST00000651053.1:n.576+132G= (NCF4)
ENST00000248899.10:c.271+132G= (NCF4)	ENSP00000248899.6:n.271+132G=
ENST00000397147.6:c.271+132G= (NCF4)	ENSP00000380334.4:n.271+132G=
ENST00000447071.5:c.-39+132G= (NCF4)	ENSP00000414958.1:n.-39+132G=
NM_000631.4:c.271+132G= (NCF4)	NP_000622.2:n.271+132G=
NM_013416.3:c.271+132G= , LRG_159t1:c.271+132G= (NCF4)	NP_038202.2:n.271+132G=
XM_011530198.1:c.445+132G= (NCF4)	XP_011528500.1:n.445+132G=
XM_011530199.1:c.415+132G= (NCF4)	XP_011528501.1:n.415+132G=
NR_147197.1:n.351+4889C= (NCF4-AS1)
XM_017028808.1:c.-39+132G= (NCF4)	XP_016884297.1:n.-39+132G=
NM_000631.5:c.271+132G= (NCF4) MANE Select	NP_000622.2:n.271+132G=
NM_013416.4:c.271+132G= (NCF4)	NP_038202.2:n.271+132G=