Canonical Allele Identifier: CA2404069461

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862372G= , CM000684.2:g.36862372G=	GRCh38
NC_000022.10:g.37258414G= , CM000684.1:g.37258414G=	GRCh37
NC_000022.9:g.35588360G=	NCBI36
NG_023400.1:g.6385G= , LRG_159:g.6385G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248899.11:c.32+1169G= (NCF4) MANE Select	ENSP00000248899.6:n.32+1169G=
ENST00000397147.7:c.32+1169G= (NCF4)	ENSP00000380334.4:n.32+1169G=
ENST00000650827.1:c.-293G= (NCF4)	ENSP00000498212.1:n.-293G=
ENST00000248899.10:c.32+1169G= (NCF4)	ENSP00000248899.6:n.32+1169G=
ENST00000397147.6:c.32+1169G= (NCF4)	ENSP00000380334.4:n.32+1169G=
ENST00000447071.5:c.-193+1169G= (NCF4)	ENSP00000414958.1:n.-193+1169G=
NM_000631.4:c.32+1169G= (NCF4)	NP_000622.2:n.32+1169G=
NM_013416.3:c.32+1169G= , LRG_159t1:c.32+1169G= (NCF4)	NP_038202.2:n.32+1169G=
XM_011530198.1:c.-283G= (NCF4)	XP_011528500.1:n.-283G=
XM_011530199.1:c.97+557G= (NCF4)	XP_011528501.1:n.97+557G=
NR_147197.1:n.351+7721C= (NCF4-AS1)
XM_017028808.1:c.-278+557G= (NCF4)	XP_016884297.1:n.-278+557G=
NM_000631.5:c.32+1169G= (NCF4) MANE Select	NP_000622.2:n.32+1169G=
NM_013416.4:c.32+1169G= (NCF4)	NP_038202.2:n.32+1169G=