Canonical Allele Identifier: CA2404069543

Gene: NCF4 NCF4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862526G= , CM000684.2:g.36862526G=	GRCh38
NC_000022.10:g.37258568G= , CM000684.1:g.37258568G=	GRCh37
NC_000022.9:g.35588514G=	NCBI36
NG_023400.1:g.6539G= , LRG_159:g.6539G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248899.11:c.32+1323G= (NCF4) MANE Select	ENSP00000248899.6:n.32+1323G=
ENST00000397147.7:c.32+1323G= (NCF4)	ENSP00000380334.4:n.32+1323G=
ENST00000650827.1:c.-278+139G= (NCF4)	ENSP00000498212.1:n.-278+139G=
ENST00000651053.1:n.3G= (NCF4)
ENST00000248899.10:c.32+1323G= (NCF4)	ENSP00000248899.6:n.32+1323G=
ENST00000397147.6:c.32+1323G= (NCF4)	ENSP00000380334.4:n.32+1323G=
ENST00000447071.5:c.-193+1323G= (NCF4)	ENSP00000414958.1:n.-193+1323G=
NM_000631.4:c.32+1323G= (NCF4)	NP_000622.2:n.32+1323G=
NM_013416.3:c.32+1323G= , LRG_159t1:c.32+1323G= (NCF4)	NP_038202.2:n.32+1323G=
XM_011530198.1:c.-129G= (NCF4)	XP_011528500.1:n.-129G=
XM_011530199.1:c.98-621G= (NCF4)	XP_011528501.1:n.98-621G=
NR_147197.1:n.351+7567C= (NCF4-AS1)
XM_017028808.1:c.-278+711G= (NCF4)	XP_016884297.1:n.-278+711G=
NM_000631.5:c.32+1323G= (NCF4) MANE Select	NP_000622.2:n.32+1323G=
NM_013416.4:c.32+1323G= (NCF4)	NP_038202.2:n.32+1323G=