Canonical Allele Identifier: CA1717693155

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789174T= , CM000669.2:g.74789174T=	GRCh38
NC_000007.13:g.74203518T= , CM000669.1:g.74203518T=	GRCh37
NC_000007.12:g.73841454T=	NCBI36
NG_009078.2:g.20211T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*14T= MANE Select	ENSP00000289473.4:n.*14T=
ENST00000289473.10:c.*14T=	ENSP00000289473.4:n.*14T=
ENST00000289473.8:c.*14T=	ENSP00000289473.4:n.*14T=
ENST00000398421.6:n.2214T=
ENST00000455062.2:n.1296T=
NM_000265.5:c.*14T=	NP_000256.4:n.*14T=
XM_005250543.3:c.*108T=	XP_005250600.2:n.*108T=
XM_011516498.1:c.*61T=	XP_011514800.1:n.*61T=
XM_011516501.1:c.*14T=	XP_011514803.1:n.*14T=
NM_000265.6:c.*14T=	NP_000256.4:n.*14T=
NM_000265.7:c.*14T= MANE Select	NP_000256.4:n.*14T=