Canonical Allele Identifier: CA323992330

Gene: NCF4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36871651G>A , CM000684.2:g.36871651G>A	GRCh38
NC_000022.10:g.37267693G>A , CM000684.1:g.37267693G>A	GRCh37
NC_000022.9:g.35597639G>A	NCBI36
NG_023400.1:g.15664G>A , LRG_159:g.15664G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000631.5:c.471-1G>A MANE Select	NP_000622.2:n.471-1G>A
ENST00000248899.11:c.471-1G>A MANE Select	ENSP00000248899.6:n.471-1G>A
NM_000631.4:c.471-1G>A	NP_000622.2:n.471-1G>A
NM_013416.3:c.471-1G>A , LRG_159t1:c.471-1G>A	NP_038202.2:n.471-1G>A
NM_013416.4:c.471-1G>A	NP_038202.2:n.471-1G>A
ENST00000248899.10:c.471-1G>A	ENSP00000248899.6:n.471-1G>A
ENST00000397147.6:c.471-1G>A	ENSP00000380334.4:n.471-1G>A
ENST00000397147.7:c.471-1G>A	ENSP00000380334.4:n.471-1G>A
ENST00000447071.5:c.162-1G>A	ENSP00000414958.1:n.162-1G>A
ENST00000650698.1:c.162-1G>A	ENSP00000498381.1:n.162-1G>A
ENST00000650827.1:c.162-1G>A	ENSP00000498212.1:n.162-1G>A
ENST00000651053.1:n.776-1G>A
XM_011530198.1:c.645-1G>A	XP_011528500.1:n.645-1G>A
XM_011530199.1:c.615-1G>A	XP_011528501.1:n.615-1G>A
XM_017028808.1:c.162-1G>A	XP_016884297.1:n.162-1G>A