Canonical Allele Identifier: CA1025509296

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs1939793107
• gnomAD v3: 22-36862306-T-A
• gnomAD v4: 22-36862306-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862306T>A , CM000684.2:g.36862306T>A	GRCh38
NC_000022.10:g.37258348T>A , CM000684.1:g.37258348T>A	GRCh37
NC_000022.9:g.35588294T>A	NCBI36
NG_023400.1:g.6319T>A , LRG_159:g.6319T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.32+1103T>A (NCF4) MANE Select	ENSP00000248899.6:n.32+1103T>A
ENST00000397147.7:c.32+1103T>A (NCF4)	ENSP00000380334.4:n.32+1103T>A
ENST00000650827.1:c.-359T>A (NCF4)	ENSP00000498212.1:n.-359T>A
ENST00000248899.10:c.32+1103T>A (NCF4)	ENSP00000248899.6:n.32+1103T>A
ENST00000397147.6:c.32+1103T>A (NCF4)	ENSP00000380334.4:n.32+1103T>A
ENST00000447071.5:c.-193+1103T>A (NCF4)	ENSP00000414958.1:n.-193+1103T>A
NM_000631.4:c.32+1103T>A (NCF4)	NP_000622.2:n.32+1103T>A
NM_013416.3:c.32+1103T>A , LRG_159t1:c.32+1103T>A (NCF4)	NP_038202.2:n.32+1103T>A
XM_011530198.1:c.-349T>A (NCF4)	XP_011528500.1:n.-349T>A
XM_011530199.1:c.97+491T>A (NCF4)	XP_011528501.1:n.97+491T>A
NR_147197.1:n.351+7787A>T (NCF4-AS1)
XM_017028808.1:c.-278+491T>A (NCF4)	XP_016884297.1:n.-278+491T>A
NM_000631.5:c.32+1103T>A (NCF4) MANE Select	NP_000622.2:n.32+1103T>A
NM_013416.4:c.32+1103T>A (NCF4)	NP_038202.2:n.32+1103T>A