Canonical Allele Identifier: CA1717693141

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789155G= , CM000669.2:g.74789155G=	GRCh38
NC_000007.13:g.74203499G= , CM000669.1:g.74203499G=	GRCh37
NC_000007.12:g.73841435G=	NCBI36
NG_009078.2:g.20192G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1168G= MANE Select	ENSP00000289473.4:p.Val390=
ENST00000289473.10:c.1168G=	ENSP00000289473.4:p.Val390=
ENST00000289473.8:c.1168G=	ENSP00000289473.4:p.Val390=
ENST00000398421.6:n.2195G=
ENST00000455062.2:n.1277G=
NM_000265.5:c.1168G=	NP_000256.4:p.Val390=
XM_005250543.3:c.*89G=	XP_005250600.2:n.*89G=
XM_011516498.1:c.*42G=	XP_011514800.1:n.*42G=
XM_011516501.1:c.775G=	XP_011514803.1:p.Val259=
NM_000265.6:c.1168G=	NP_000256.4:p.Val390=
NM_000265.7:c.1168G= MANE Select	NP_000256.4:p.Val390=