Canonical Allele Identifier: CA10212936

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs387906808
• ExAC: 22:37263476 G / T
• gnomAD v2: 22-37263476-G-T
• MyVariant Identifiers: chr22:g.37263476G>T (hg19) ; chr22:g.36867434G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36867434G>T , CM000684.2:g.36867434G>T	GRCh38
NC_000022.10:g.37263476G>T , CM000684.1:g.37263476G>T	GRCh37
NC_000022.9:g.35593422G>T	NCBI36
NG_023400.1:g.11447G>T , LRG_159:g.11447G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000248899.11:c.314G>T (NCF4) MANE Select	ENSP00000248899.6:p.Arg105Leu
ENST00000397147.7:c.314G>T (NCF4)	ENSP00000380334.4:p.Arg105Leu
ENST00000650698.1:c.5G>T (NCF4)	ENSP00000498381.1:p.Arg2Leu
ENST00000650827.1:c.5G>T (NCF4)	ENSP00000498212.1:p.Arg2Leu
ENST00000651053.1:n.619G>T (NCF4)
ENST00000248899.10:c.314G>T (NCF4)	ENSP00000248899.6:p.Arg105Leu
ENST00000397147.6:c.314G>T (NCF4)	ENSP00000380334.4:p.Arg105Leu
ENST00000447071.5:c.5G>T (NCF4)	ENSP00000414958.1:p.Arg2Leu
NM_000631.4:c.314G>T (NCF4)	NP_000622.2:p.Arg105Leu
NM_013416.3:c.314G>T , LRG_159t1:c.314G>T (NCF4)	NP_038202.2:p.Arg105Leu
XM_011530198.1:c.488G>T (NCF4)	XP_011528500.1:p.Arg163Leu
XM_011530199.1:c.458G>T (NCF4)	XP_011528501.1:p.Arg153Leu
NR_147197.1:n.351+2659C>A (NCF4-AS1)
XM_017028808.1:c.5G>T (NCF4)	XP_016884297.1:p.Arg2Leu
NM_000631.5:c.314G>T (NCF4) MANE Select	NP_000622.2:p.Arg105Leu
NM_013416.4:c.314G>T (NCF4)	NP_038202.2:p.Arg105Leu