Canonical Allele Identifier: CA1717693144

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789161G= , CM000669.2:g.74789161G=	GRCh38
NC_000007.13:g.74203505G= , CM000669.1:g.74203505G=	GRCh37
NC_000007.12:g.73841441G=	NCBI36
NG_009078.2:g.20198G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*1G= MANE Select	ENSP00000289473.4:n.*1G=
ENST00000289473.10:c.*1G=	ENSP00000289473.4:n.*1G=
ENST00000289473.8:c.*1G=	ENSP00000289473.4:n.*1G=
ENST00000398421.6:n.2201G=
ENST00000455062.2:n.1283G=
NM_000265.5:c.*1G=	NP_000256.4:n.*1G=
XM_005250543.3:c.*95G=	XP_005250600.2:n.*95G=
XM_011516498.1:c.*48G=	XP_011514800.1:n.*48G=
XM_011516501.1:c.*1G=	XP_011514803.1:n.*1G=
NM_000265.6:c.*1G=	NP_000256.4:n.*1G=
NM_000265.7:c.*1G= MANE Select	NP_000256.4:n.*1G=