Canonical Allele Identifier: CA1717693161

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789180G= , CM000669.2:g.74789180G=	GRCh38
NC_000007.13:g.74203524G= , CM000669.1:g.74203524G=	GRCh37
NC_000007.12:g.73841460G=	NCBI36
NG_009078.2:g.20217G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*20G= MANE Select	ENSP00000289473.4:n.*20G=
ENST00000289473.10:c.*20G=	ENSP00000289473.4:n.*20G=
ENST00000289473.8:c.*20G=	ENSP00000289473.4:n.*20G=
ENST00000398421.6:n.2220G=
ENST00000455062.2:n.1302G=
NM_000265.5:c.*20G=	NP_000256.4:n.*20G=
XM_005250543.3:c.*114G=	XP_005250600.2:n.*114G=
XM_011516498.1:c.*67G=	XP_011514800.1:n.*67G=
XM_011516501.1:c.*20G=	XP_011514803.1:n.*20G=
NM_000265.6:c.*20G=	NP_000256.4:n.*20G=
NM_000265.7:c.*20G= MANE Select	NP_000256.4:n.*20G=