Canonical Allele Identifier: CA1717689869

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74783436T= , CM000669.2:g.74783436T=	GRCh38
NC_000007.13:g.74197779T= , CM000669.1:g.74197779T=	GRCh37
NC_000007.12:g.73835715T=	NCBI36
NG_009078.2:g.14473T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.575-89T= MANE Select	ENSP00000289473.4:n.575-89T=
ENST00000289473.10:c.575-89T=	ENSP00000289473.4:n.575-89T=
ENST00000289473.8:c.575-89T=	ENSP00000289473.4:n.575-89T=
ENST00000398421.6:n.1043T=
ENST00000443956.7:n.696-89T=
ENST00000449343.6:n.970T=
ENST00000455062.2:n.633T=
ENST00000464878.5:c.799T=
NM_000265.5:c.575-89T=	NP_000256.4:n.575-89T=
XM_005250543.3:c.575-89T=	XP_005250600.2:n.575-89T=
XM_005250544.3:c.575-89T=	XP_005250601.2:n.575-89T=
XM_011516498.1:c.575-89T=	XP_011514800.1:n.575-89T=
XM_011516499.1:c.575-89T=	XP_011514801.1:n.575-89T=
XM_011516500.1:c.575-89T=	XP_011514802.1:n.575-89T=
XM_011516501.1:c.182-89T=	XP_011514803.1:n.182-89T=
XR_242262.3:n.630-89T=
XR_927515.1:n.630-89T=
NM_000265.6:c.575-89T=	NP_000256.4:n.575-89T=
NM_000265.7:c.575-89T= MANE Select	NP_000256.4:n.575-89T=