Canonical Allele Identifier: CA1717693209

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789227A= , CM000669.2:g.74789227A=	GRCh38
NC_000007.13:g.74203571A= , CM000669.1:g.74203571A=	GRCh37
NC_000007.12:g.73841507A=	NCBI36
NG_009078.2:g.20264A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000289473.11:c.*67A= MANE Select	ENSP00000289473.4:n.*67A=
ENST00000289473.10:c.*67A=	ENSP00000289473.4:n.*67A=
ENST00000289473.8:c.*67A=	ENSP00000289473.4:n.*67A=
ENST00000398421.6:n.2267A=
ENST00000455062.2:n.1349A=
NM_000265.5:c.*67A=	NP_000256.4:n.*67A=
XM_005250543.3:c.*161A=	XP_005250600.2:n.*161A=
XM_011516498.1:c.*114A=	XP_011514800.1:n.*114A=
XM_011516501.1:c.*67A=	XP_011514803.1:n.*67A=
NM_000265.6:c.*67A=	NP_000256.4:n.*67A=
NM_000265.7:c.*67A= MANE Select	NP_000256.4:n.*67A=