Canonical Allele Identifier: CA1717693179

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789205C= , CM000669.2:g.74789205C=	GRCh38
NC_000007.13:g.74203549C= , CM000669.1:g.74203549C=	GRCh37
NC_000007.12:g.73841485C=	NCBI36
NG_009078.2:g.20242C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000289473.11:c.*45C= MANE Select	ENSP00000289473.4:n.*45C=
ENST00000289473.10:c.*45C=	ENSP00000289473.4:n.*45C=
ENST00000289473.8:c.*45C=	ENSP00000289473.4:n.*45C=
ENST00000398421.6:n.2245C=
ENST00000455062.2:n.1327C=
NM_000265.5:c.*45C=	NP_000256.4:n.*45C=
XM_005250543.3:c.*139C=	XP_005250600.2:n.*139C=
XM_011516498.1:c.*92C=	XP_011514800.1:n.*92C=
XM_011516501.1:c.*45C=	XP_011514803.1:n.*45C=
NM_000265.6:c.*45C=	NP_000256.4:n.*45C=
NM_000265.7:c.*45C= MANE Select	NP_000256.4:n.*45C=