Canonical Allele Identifier: CA323990578

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36870076G>A , CM000684.2:g.36870076G>A	GRCh38
NC_000022.10:g.37266118G>A , CM000684.1:g.37266118G>A	GRCh37
NC_000022.9:g.35596064G>A	NCBI36
NG_023400.1:g.14089G>A , LRG_159:g.14089G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000631.5:c.343-339G>A (NCF4) MANE Select	NP_000622.2:n.343-339G>A
ENST00000248899.11:c.343-339G>A (NCF4) MANE Select	ENSP00000248899.6:n.343-339G>A
NM_000631.4:c.343-339G>A (NCF4)	NP_000622.2:n.343-339G>A
NM_013416.3:c.343-339G>A , LRG_159t1:c.343-339G>A (NCF4)	NP_038202.2:n.343-339G>A
NM_013416.4:c.343-339G>A (NCF4)	NP_038202.2:n.343-339G>A
NR_147197.1:n.351+17C>T (NCF4-AS1)
ENST00000248899.10:c.343-339G>A (NCF4)	ENSP00000248899.6:n.343-339G>A
ENST00000397147.6:c.343-339G>A (NCF4)	ENSP00000380334.4:n.343-339G>A
ENST00000397147.7:c.343-339G>A (NCF4)	ENSP00000380334.4:n.343-339G>A
ENST00000447071.5:c.34-339G>A (NCF4)	ENSP00000414958.1:n.34-339G>A
ENST00000650698.1:c.34-339G>A (NCF4)	ENSP00000498381.1:n.34-339G>A
ENST00000650827.1:c.34-339G>A (NCF4)	ENSP00000498212.1:n.34-339G>A
ENST00000651053.1:n.648-339G>A (NCF4)
XM_011530198.1:c.517-339G>A (NCF4)	XP_011528500.1:n.517-339G>A
XM_011530199.1:c.487-339G>A (NCF4)	XP_011528501.1:n.487-339G>A
XM_017028808.1:c.34-339G>A (NCF4)	XP_016884297.1:n.34-339G>A