Canonical Allele Identifier: CA1717693035

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789061C= , CM000669.2:g.74789061C=	GRCh38
NC_000007.13:g.74203405C= , CM000669.1:g.74203405C=	GRCh37
NC_000007.12:g.73841341C=	NCBI36
NG_009078.2:g.20098C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1074C= MANE Select	ENSP00000289473.4:p.Arg358=
ENST00000289473.10:c.1074C=	ENSP00000289473.4:p.Arg358=
ENST00000289473.8:c.1074C=	ENSP00000289473.4:p.Arg358=
ENST00000398421.6:n.2101C=
ENST00000455062.2:n.1183C=
NM_000265.5:c.1074C=	NP_000256.4:p.Arg358=
XM_005250543.3:c.1036C=	XP_005250600.2:p.Leu346=
XM_011516498.1:c.1073C=	XP_011514800.1:p.Ala358=
XM_011516501.1:c.681C=	XP_011514803.1:p.Arg227=
NM_000265.6:c.1074C=	NP_000256.4:p.Arg358=
NM_000265.7:c.1074C= MANE Select	NP_000256.4:p.Arg358=