Canonical Allele Identifier: CA411379304

Gene: NCF4 NCF4-AS1

Linked Data

• MyVariant Identifiers: chr22:g.37261067C>G (hg19) ; chr22:g.36865025C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36865025C>G , CM000684.2:g.36865025C>G	GRCh38
NC_000022.10:g.37261067C>G , CM000684.1:g.37261067C>G	GRCh37
NC_000022.9:g.35591013C>G	NCBI36
NG_023400.1:g.9038C>G , LRG_159:g.9038C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.224C>G (NCF4) MANE Select	ENSP00000248899.6:p.Pro75Arg
ENST00000397147.7:c.224C>G (NCF4)	ENSP00000380334.4:p.Pro75Arg
ENST00000650698.1:c.-86C>G (NCF4)	ENSP00000498381.1:n.-86C>G
ENST00000650827.1:c.-86C>G (NCF4)	ENSP00000498212.1:n.-86C>G
ENST00000651053.1:n.529C>G (NCF4)
ENST00000248899.10:c.224C>G (NCF4)	ENSP00000248899.6:p.Pro75Arg
ENST00000397147.6:c.224C>G (NCF4)	ENSP00000380334.4:p.Pro75Arg
ENST00000447071.5:c.-86C>G (NCF4)	ENSP00000414958.1:n.-86C>G
NM_000631.4:c.224C>G (NCF4)	NP_000622.2:p.Pro75Arg
NM_013416.3:c.224C>G , LRG_159t1:c.224C>G (NCF4)	NP_038202.2:p.Pro75Arg
XM_011530198.1:c.398C>G (NCF4)	XP_011528500.1:p.Pro133Arg
XM_011530199.1:c.368C>G (NCF4)	XP_011528501.1:p.Pro123Arg
NR_147197.1:n.351+5068G>C (NCF4-AS1)
XM_017028808.1:c.-86C>G (NCF4)	XP_016884297.1:n.-86C>G
NM_000631.5:c.224C>G (NCF4) MANE Select	NP_000622.2:p.Pro75Arg
NM_013416.4:c.224C>G (NCF4)	NP_038202.2:p.Pro75Arg