Canonical Allele Identifier: CA1717693197

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789216A= , CM000669.2:g.74789216A=	GRCh38
NC_000007.13:g.74203560A= , CM000669.1:g.74203560A=	GRCh37
NC_000007.12:g.73841496A=	NCBI36
NG_009078.2:g.20253A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000289473.11:c.*56A= MANE Select	ENSP00000289473.4:n.*56A=
ENST00000289473.10:c.*56A=	ENSP00000289473.4:n.*56A=
ENST00000289473.8:c.*56A=	ENSP00000289473.4:n.*56A=
ENST00000398421.6:n.2256A=
ENST00000455062.2:n.1338A=
NM_000265.5:c.*56A=	NP_000256.4:n.*56A=
XM_005250543.3:c.*150A=	XP_005250600.2:n.*150A=
XM_011516498.1:c.*103A=	XP_011514800.1:n.*103A=
XM_011516501.1:c.*56A=	XP_011514803.1:n.*56A=
NM_000265.6:c.*56A=	NP_000256.4:n.*56A=
NM_000265.7:c.*56A= MANE Select	NP_000256.4:n.*56A=