Canonical Allele Identifier: CA2404069419

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862294T= , CM000684.2:g.36862294T=	GRCh38
NC_000022.10:g.37258336T= , CM000684.1:g.37258336T=	GRCh37
NC_000022.9:g.35588282T=	NCBI36
NG_023400.1:g.6307T= , LRG_159:g.6307T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.32+1091T= (NCF4) MANE Select	ENSP00000248899.6:n.32+1091T=
ENST00000397147.7:c.32+1091T= (NCF4)	ENSP00000380334.4:n.32+1091T=
ENST00000248899.10:c.32+1091T= (NCF4)	ENSP00000248899.6:n.32+1091T=
ENST00000397147.6:c.32+1091T= (NCF4)	ENSP00000380334.4:n.32+1091T=
ENST00000447071.5:c.-193+1091T= (NCF4)	ENSP00000414958.1:n.-193+1091T=
NM_000631.4:c.32+1091T= (NCF4)	NP_000622.2:n.32+1091T=
NM_013416.3:c.32+1091T= , LRG_159t1:c.32+1091T= (NCF4)	NP_038202.2:n.32+1091T=
XM_011530198.1:c.-361T= (NCF4)	XP_011528500.1:n.-361T=
XM_011530199.1:c.97+479T= (NCF4)	XP_011528501.1:n.97+479T=
NR_147197.1:n.351+7799A= (NCF4-AS1)
XM_017028808.1:c.-278+479T= (NCF4)	XP_016884297.1:n.-278+479T=
NM_000631.5:c.32+1091T= (NCF4) MANE Select	NP_000622.2:n.32+1091T=
NM_013416.4:c.32+1091T= (NCF4)	NP_038202.2:n.32+1091T=