Canonical Allele Identifier: CA1717693238

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789282C= , CM000669.2:g.74789282C=	GRCh38
NC_000007.13:g.74203626C= , CM000669.1:g.74203626C=	GRCh37
NC_000007.12:g.73841562C=	NCBI36
NG_009078.2:g.20319C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*122C= MANE Select	ENSP00000289473.4:n.*122C=
ENST00000289473.10:c.*122C=	ENSP00000289473.4:n.*122C=
ENST00000289473.8:c.*122C=	ENSP00000289473.4:n.*122C=
ENST00000398421.6:n.2322C=
ENST00000455062.2:n.1404C=
NM_000265.5:c.*122C=	NP_000256.4:n.*122C=
XM_005250543.3:c.*216C=	XP_005250600.2:n.*216C=
XM_011516498.1:c.*169C=	XP_011514800.1:n.*169C=
XM_011516501.1:c.*122C=	XP_011514803.1:n.*122C=
NM_000265.6:c.*122C=	NP_000256.4:n.*122C=
NM_000265.7:c.*122C= MANE Select	NP_000256.4:n.*122C=