Canonical Allele Identifier: CA1717692890

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74788995_74788996delinsGT , CM000669.2:g.74788995_74788996delinsGT	GRCh38
NG_009078.2:g.20032_20033delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1052-44_1052-43delinsGT MANE Select	ENSP00000289473.4:n.1052-44_1052-43delinsGT
ENST00000289473.10:c.1052-44_1052-43delinsGT	ENSP00000289473.4:n.1052-44_1052-43delinsGT
ENST00000289473.8:c.1052-44_1052-43delinsGT	ENSP00000289473.4:n.1052-44_1052-43delinsGT
ENST00000398421.6:n.2079-44_2079-43delinsGT
ENST00000455062.2:n.1161-44_1161-43delinsGT
NM_000265.5:c.1052-44_1052-43delinsGT	NP_000256.4:n.1052-44_1052-43delinsGT
XM_005250543.3:c.1014-44_1014-43delinsGT	XP_005250600.2:n.1014-44_1014-43delinsGT
XM_011516498.1:c.1051-44_1051-43delinsGT	XP_011514800.1:n.1051-44_1051-43delinsGT
XM_011516501.1:c.659-44_659-43delinsGT	XP_011514803.1:n.659-44_659-43delinsGT
NM_000265.6:c.1052-44_1052-43delinsGT	NP_000256.4:n.1052-44_1052-43delinsGT
NM_000265.7:c.1052-44_1052-43delinsGT MANE Select	NP_000256.4:n.1052-44_1052-43delinsGT