Canonical Allele Identifier: CA115440

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74777319G>A , CM000669.2:g.74777319G>A	GRCh38
NC_000007.13:g.74191665G>A , CM000669.1:g.74191665G>A	GRCh37
NC_000007.12:g.73829601G>A	NCBI36
NG_009078.2:g.8356G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.125G>A MANE Select	ENSP00000289473.4:p.Arg42Gln
ENST00000289473.10:c.125G>A	ENSP00000289473.4:p.Arg42Gln
ENST00000289473.8:c.125G>A	ENSP00000289473.4:p.Arg42Gln
ENST00000398421.6:n.146G>A
ENST00000433458.5:c.51G>A
ENST00000438106.5:n.53G>A
ENST00000442021.6:c.51G>A
ENST00000443956.7:n.98G>A
ENST00000449343.6:n.146G>A
ENST00000455062.2:n.51G>A
ENST00000464878.5:c.51G>A
NM_000265.5:c.125G>A	NP_000256.4:p.Arg42Gln
XM_005250543.3:c.125G>A	XP_005250600.2:p.Arg42Gln
XM_005250544.3:c.125G>A	XP_005250601.2:p.Arg42Gln
XM_011516498.1:c.125G>A	XP_011514800.1:p.Arg42Gln
XM_011516499.1:c.125G>A	XP_011514801.1:p.Arg42Gln
XM_011516500.1:c.125G>A	XP_011514802.1:p.Arg42Gln
XM_011516501.1:c.-27G>A	XP_011514803.1:n.-27G>A
XR_242262.3:n.180G>A
XR_927515.1:n.180G>A
NM_000265.6:c.125G>A	NP_000256.4:p.Arg42Gln
NM_000265.7:c.125G>A MANE Select	NP_000256.4:p.Arg42Gln