Canonical Allele Identifier: CA1717689912

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74783528G= , CM000669.2:g.74783528G=	GRCh38
NC_000007.13:g.74197871G= , CM000669.1:g.74197871G=	GRCh37
NC_000007.12:g.73835807G=	NCBI36
NG_009078.2:g.14565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.578G= MANE Select	ENSP00000289473.4:p.Trp193=
ENST00000289473.10:c.578G=	ENSP00000289473.4:p.Trp193=
ENST00000289473.8:c.578G=	ENSP00000289473.4:p.Trp193=
ENST00000398421.6:n.1135G=
ENST00000443956.7:n.699G=
ENST00000449343.6:n.1062G=
ENST00000455062.2:n.725G=
ENST00000464878.5:c.891G=
ENST00000486097.1:n.86G=
NM_000265.5:c.578G=	NP_000256.4:p.Trp193=
XM_005250543.3:c.578G=	XP_005250600.2:p.Trp193=
XM_005250544.3:c.578G=	XP_005250601.2:p.Trp193=
XM_011516498.1:c.578G=	XP_011514800.1:p.Trp193=
XM_011516499.1:c.578G=	XP_011514801.1:p.Trp193=
XM_011516500.1:c.578G=	XP_011514802.1:p.Trp193=
XM_011516501.1:c.185G=	XP_011514803.1:p.Trp62=
XR_242262.3:n.633G=
XR_927515.1:n.633G=
NM_000265.6:c.578G=	NP_000256.4:p.Trp193=
NM_000265.7:c.578G= MANE Select	NP_000256.4:p.Trp193=