Canonical Allele Identifier: CA1717693150

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789171C= , CM000669.2:g.74789171C=	GRCh38
NC_000007.13:g.74203515C= , CM000669.1:g.74203515C=	GRCh37
NC_000007.12:g.73841451C=	NCBI36
NG_009078.2:g.20208C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000289473.11:c.*11C= MANE Select	ENSP00000289473.4:n.*11C=
ENST00000289473.10:c.*11C=	ENSP00000289473.4:n.*11C=
ENST00000289473.8:c.*11C=	ENSP00000289473.4:n.*11C=
ENST00000398421.6:n.2211C=
ENST00000455062.2:n.1293C=
NM_000265.5:c.*11C=	NP_000256.4:n.*11C=
XM_005250543.3:c.*105C=	XP_005250600.2:n.*105C=
XM_011516498.1:c.*58C=	XP_011514800.1:n.*58C=
XM_011516501.1:c.*11C=	XP_011514803.1:n.*11C=
NM_000265.6:c.*11C=	NP_000256.4:n.*11C=
NM_000265.7:c.*11C= MANE Select	NP_000256.4:n.*11C=