Canonical Allele Identifier: CA2557385061

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862396G>A , CM000684.2:g.36862396G>A	GRCh38
NC_000022.10:g.37258438G>A , CM000684.1:g.37258438G>A	GRCh37
NC_000022.9:g.35588384G>A	NCBI36
NG_023400.1:g.6409G>A , LRG_159:g.6409G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248899.11:c.32+1193G>A (NCF4) MANE Select	ENSP00000248899.6:n.32+1193G>A
ENST00000397147.7:c.32+1193G>A (NCF4)	ENSP00000380334.4:n.32+1193G>A
ENST00000650827.1:c.-278+9G>A (NCF4)	ENSP00000498212.1:n.-278+9G>A
ENST00000248899.10:c.32+1193G>A (NCF4)	ENSP00000248899.6:n.32+1193G>A
ENST00000397147.6:c.32+1193G>A (NCF4)	ENSP00000380334.4:n.32+1193G>A
ENST00000447071.5:c.-193+1193G>A (NCF4)	ENSP00000414958.1:n.-193+1193G>A
NM_000631.4:c.32+1193G>A (NCF4)	NP_000622.2:n.32+1193G>A
NM_013416.3:c.32+1193G>A , LRG_159t1:c.32+1193G>A (NCF4)	NP_038202.2:n.32+1193G>A
XM_011530198.1:c.-259G>A (NCF4)	XP_011528500.1:n.-259G>A
XM_011530199.1:c.97+581G>A (NCF4)	XP_011528501.1:n.97+581G>A
NR_147197.1:n.351+7697C>T (NCF4-AS1)
XM_017028808.1:c.-278+581G>A (NCF4)	XP_016884297.1:n.-278+581G>A
NM_000631.5:c.32+1193G>A (NCF4) MANE Select	NP_000622.2:n.32+1193G>A
NM_013416.4:c.32+1193G>A (NCF4)	NP_038202.2:n.32+1193G>A