Canonical Allele Identifier: CA1717692926

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789007G= , CM000669.2:g.74789007G=	GRCh38
NC_000007.13:g.74203351G= , CM000669.1:g.74203351G=	GRCh37
NC_000007.12:g.73841287G=	NCBI36
NG_009078.2:g.20044G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1052-32G= MANE Select	ENSP00000289473.4:n.1052-32G=
ENST00000289473.10:c.1052-32G=	ENSP00000289473.4:n.1052-32G=
ENST00000289473.8:c.1052-32G=	ENSP00000289473.4:n.1052-32G=
ENST00000398421.6:n.2079-32G=
ENST00000455062.2:n.1161-32G=
NM_000265.5:c.1052-32G=	NP_000256.4:n.1052-32G=
XM_005250543.3:c.1014-32G=	XP_005250600.2:n.1014-32G=
XM_011516498.1:c.1051-32G=	XP_011514800.1:n.1051-32G=
XM_011516501.1:c.659-32G=	XP_011514803.1:n.659-32G=
NM_000265.6:c.1052-32G=	NP_000256.4:n.1052-32G=
NM_000265.7:c.1052-32G= MANE Select	NP_000256.4:n.1052-32G=