Canonical Allele Identifier: CA2683317900

Gene: NCF1

Linked Data

• gnomAD v4: 7-74788958-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74788962del , CM000669.2:g.74788962del	GRCh38
NC_000007.13:g.74203306del , CM000669.1:g.74203306del	GRCh37
NC_000007.12:g.73841242del	NCBI36
NG_009078.2:g.19999del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1052-77del MANE Select	ENSP00000289473.4:n.1052-77del
ENST00000289473.10:c.1052-77del	ENSP00000289473.4:n.1052-77del
ENST00000289473.8:c.1052-77del	ENSP00000289473.4:n.1052-77del
ENST00000398421.6:n.2079-77del
ENST00000455062.2:n.1161-77del
NM_000265.5:c.1052-77del	NP_000256.4:n.1052-77del
XM_005250543.3:c.1014-77del	XP_005250600.2:n.1014-77del
XM_011516498.1:c.1051-77del	XP_011514800.1:n.1051-77del
XM_011516501.1:c.659-77del	XP_011514803.1:n.659-77del
NM_000265.6:c.1052-77del	NP_000256.4:n.1052-77del
NM_000265.7:c.1052-77del MANE Select	NP_000256.4:n.1052-77del