Canonical Allele Identifier: CA1717688505

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74779360T= , CM000669.2:g.74779360T=	GRCh38
NC_000007.13:g.74193706T= , CM000669.1:g.74193706T=	GRCh37
NC_000007.12:g.73831642T=	NCBI36
NG_009078.2:g.10397T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000265.7:c.333T= MANE Select	NP_000256.4:p.Cys111=
ENST00000289473.11:c.333T= MANE Select	ENSP00000289473.4:p.Cys111=
NM_000265.5:c.333T=	NP_000256.4:p.Cys111=
NM_000265.6:c.333T=	NP_000256.4:p.Cys111=
ENST00000289473.10:c.333T=	ENSP00000289473.4:p.Cys111=
ENST00000289473.8:c.333T=	ENSP00000289473.4:p.Cys111=
ENST00000398421.6:n.427T=
ENST00000433458.5:c.259T=
ENST00000438106.5:n.261T=
ENST00000442021.6:c.352T=
ENST00000443956.7:n.454T=
ENST00000449343.6:n.354T=
ENST00000455062.2:n.80-1420T=
ENST00000464878.5:c.183T=
XM_005250543.3:c.333T=	XP_005250600.2:p.Cys111=
XM_005250544.3:c.333T=	XP_005250601.2:p.Cys111=
XM_011516498.1:c.333T=	XP_011514800.1:p.Cys111=
XM_011516499.1:c.333T=	XP_011514801.1:p.Cys111=
XM_011516500.1:c.333T=	XP_011514802.1:p.Cys111=
XM_011516501.1:c.3-1420T=	XP_011514803.1:n.3-1420T=
XR_242262.3:n.388T=
XR_927515.1:n.388T=