Canonical Allele Identifier: CA1717693021

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789048G= , CM000669.2:g.74789048G=	GRCh38
NC_000007.13:g.74203392G= , CM000669.1:g.74203392G=	GRCh37
NC_000007.12:g.73841328G=	NCBI36
NG_009078.2:g.20085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1061G= MANE Select	ENSP00000289473.4:p.Arg354=
ENST00000289473.10:c.1061G=	ENSP00000289473.4:p.Arg354=
ENST00000289473.8:c.1061G=	ENSP00000289473.4:p.Arg354=
ENST00000398421.6:n.2088G=
ENST00000455062.2:n.1170G=
NM_000265.5:c.1061G=	NP_000256.4:p.Arg354=
XM_005250543.3:c.1023G=	XP_005250600.2:p.Ala341=
XM_011516498.1:c.1060G=	XP_011514800.1:p.Gly354=
XM_011516501.1:c.668G=	XP_011514803.1:p.Arg223=
NM_000265.6:c.1061G=	NP_000256.4:p.Arg354=
NM_000265.7:c.1061G= MANE Select	NP_000256.4:p.Arg354=