Canonical Allele Identifier: CA1717693038

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789063C= , CM000669.2:g.74789063C=	GRCh38
NC_000007.13:g.74203407C= , CM000669.1:g.74203407C=	GRCh37
NC_000007.12:g.73841343C=	NCBI36
NG_009078.2:g.20100C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1076C= MANE Select	ENSP00000289473.4:p.Ser359=
ENST00000289473.10:c.1076C=	ENSP00000289473.4:p.Ser359=
ENST00000289473.8:c.1076C=	ENSP00000289473.4:p.Ser359=
ENST00000398421.6:n.2103C=
ENST00000455062.2:n.1185C=
NM_000265.5:c.1076C=	NP_000256.4:p.Ser359=
XM_005250543.3:c.1038C=	XP_005250600.2:p.Leu346=
XM_011516498.1:c.1075C=	XP_011514800.1:p.Leu359=
XM_011516501.1:c.683C=	XP_011514803.1:p.Ser228=
NM_000265.6:c.1076C=	NP_000256.4:p.Ser359=
NM_000265.7:c.1076C= MANE Select	NP_000256.4:p.Ser359=