Canonical Allele Identifier: CA411379319

Gene: NCF4 NCF4-AS1

Linked Data

• MyVariant Identifiers: chr22:g.37261070A>T (hg19) ; chr22:g.36865028A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36865028A>T , CM000684.2:g.36865028A>T	GRCh38
NC_000022.10:g.37261070A>T , CM000684.1:g.37261070A>T	GRCh37
NC_000022.9:g.35591016A>T	NCBI36
NG_023400.1:g.9041A>T , LRG_159:g.9041A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.227A>T (NCF4) MANE Select	ENSP00000248899.6:p.Asp76Val
ENST00000397147.7:c.227A>T (NCF4)	ENSP00000380334.4:p.Asp76Val
ENST00000650698.1:c.-83A>T (NCF4)	ENSP00000498381.1:n.-83A>T
ENST00000650827.1:c.-83A>T (NCF4)	ENSP00000498212.1:n.-83A>T
ENST00000651053.1:n.532A>T (NCF4)
ENST00000248899.10:c.227A>T (NCF4)	ENSP00000248899.6:p.Asp76Val
ENST00000397147.6:c.227A>T (NCF4)	ENSP00000380334.4:p.Asp76Val
ENST00000447071.5:c.-83A>T (NCF4)	ENSP00000414958.1:n.-83A>T
NM_000631.4:c.227A>T (NCF4)	NP_000622.2:p.Asp76Val
NM_013416.3:c.227A>T , LRG_159t1:c.227A>T (NCF4)	NP_038202.2:p.Asp76Val
XM_011530198.1:c.401A>T (NCF4)	XP_011528500.1:p.Asp134Val
XM_011530199.1:c.371A>T (NCF4)	XP_011528501.1:p.Asp124Val
NR_147197.1:n.351+5065T>A (NCF4-AS1)
XM_017028808.1:c.-83A>T (NCF4)	XP_016884297.1:n.-83A>T
NM_000631.5:c.227A>T (NCF4) MANE Select	NP_000622.2:p.Asp76Val
NM_013416.4:c.227A>T (NCF4)	NP_038202.2:p.Asp76Val