Canonical Allele Identifier: CA2683317865

Gene: NCF1

Linked Data

• gnomAD v4: 7-74788896-C-CAGAGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74788902_74788907dup , CM000669.2:g.74788902_74788907dup	GRCh38
NC_000007.13:g.74203246_74203251dup , CM000669.1:g.74203246_74203251dup	GRCh37
NC_000007.12:g.73841182_73841187dup	NCBI36
NG_009078.2:g.19939_19944dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1052-137_1052-132dup MANE Select	ENSP00000289473.4:n.1052-137_1052-132dup
ENST00000289473.10:c.1052-137_1052-132dup	ENSP00000289473.4:n.1052-137_1052-132dup
ENST00000289473.8:c.1052-137_1052-132dup	ENSP00000289473.4:n.1052-137_1052-132dup
ENST00000398421.6:n.2079-137_2079-132dup
ENST00000455062.2:n.1161-137_1161-132dup
NM_000265.5:c.1052-137_1052-132dup	NP_000256.4:n.1052-137_1052-132dup
XM_005250543.3:c.1014-137_1014-132dup	XP_005250600.2:n.1014-137_1014-132dup
XM_011516498.1:c.1051-137_1051-132dup	XP_011514800.1:n.1051-137_1051-132dup
XM_011516501.1:c.659-137_659-132dup	XP_011514803.1:n.659-137_659-132dup
NM_000265.6:c.1052-137_1052-132dup	NP_000256.4:n.1052-137_1052-132dup
NM_000265.7:c.1052-137_1052-132dup MANE Select	NP_000256.4:n.1052-137_1052-132dup