Canonical Allele Identifier: CA411376246

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36864044G>A , CM000684.2:g.36864044G>A	GRCh38
NC_000022.10:g.37260086G>A , CM000684.1:g.37260086G>A	GRCh37
NC_000022.9:g.35590032G>A	NCBI36
NG_023400.1:g.8057G>A , LRG_159:g.8057G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000631.5:c.33-1G>A (NCF4) MANE Select	NP_000622.2:n.33-1G>A
ENST00000248899.11:c.33-1G>A (NCF4) MANE Select	ENSP00000248899.6:n.33-1G>A
NM_000631.4:c.33-1G>A (NCF4)	NP_000622.2:n.33-1G>A
NM_013416.3:c.33-1G>A , LRG_159t1:c.33-1G>A (NCF4)	NP_038202.2:n.33-1G>A
NM_013416.4:c.33-1G>A (NCF4)	NP_038202.2:n.33-1G>A
NR_147197.1:n.351+6049C>T (NCF4-AS1)
ENST00000248899.10:c.33-1G>A (NCF4)	ENSP00000248899.6:n.33-1G>A
ENST00000397147.6:c.33-1G>A (NCF4)	ENSP00000380334.4:n.33-1G>A
ENST00000397147.7:c.33-1G>A (NCF4)	ENSP00000380334.4:n.33-1G>A
ENST00000447071.5:c.-192-875G>A (NCF4)	ENSP00000414958.1:n.-192-875G>A
ENST00000650698.1:c.-277-1G>A (NCF4)	ENSP00000498381.1:n.-277-1G>A
ENST00000650827.1:c.-277-1G>A (NCF4)	ENSP00000498212.1:n.-277-1G>A
ENST00000651053.1:n.338-1G>A (NCF4)
XM_011530198.1:c.207-1G>A (NCF4)	XP_011528500.1:n.207-1G>A
XM_011530199.1:c.177-1G>A (NCF4)	XP_011528501.1:n.177-1G>A
XM_017028808.1:c.-277-1G>A (NCF4)	XP_016884297.1:n.-277-1G>A