Canonical Allele Identifier: CA1717693251

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789294A= , CM000669.2:g.74789294A=	GRCh38
NC_000007.13:g.74203638A= , CM000669.1:g.74203638A=	GRCh37
NC_000007.12:g.73841574A=	NCBI36
NG_009078.2:g.20331A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000289473.11:c.*134A= MANE Select	ENSP00000289473.4:n.*134A=
ENST00000289473.10:c.*134A=	ENSP00000289473.4:n.*134A=
ENST00000289473.8:c.*134A=	ENSP00000289473.4:n.*134A=
ENST00000398421.6:n.2334A=
ENST00000455062.2:n.1416A=
NM_000265.5:c.*134A=	NP_000256.4:n.*134A=
XM_005250543.3:c.*228A=	XP_005250600.2:n.*228A=
XM_011516498.1:c.*181A=	XP_011514800.1:n.*181A=
XM_011516501.1:c.*134A=	XP_011514803.1:n.*134A=
NM_000265.6:c.*134A=	NP_000256.4:n.*134A=
NM_000265.7:c.*134A= MANE Select	NP_000256.4:n.*134A=