Canonical Allele Identifier: CA2683317872

Gene: NCF1

Linked Data

• gnomAD v4: 7-74788901-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74788905_74788906dup , CM000669.2:g.74788905_74788906dup	GRCh38
NC_000007.13:g.74203249_74203250dup , CM000669.1:g.74203249_74203250dup	GRCh37
NC_000007.12:g.73841185_73841186dup	NCBI36
NG_009078.2:g.19942_19943dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1052-134_1052-133dup MANE Select	ENSP00000289473.4:n.1052-134_1052-133dup
ENST00000289473.10:c.1052-134_1052-133dup	ENSP00000289473.4:n.1052-134_1052-133dup
ENST00000289473.8:c.1052-134_1052-133dup	ENSP00000289473.4:n.1052-134_1052-133dup
ENST00000398421.6:n.2079-134_2079-133dup
ENST00000455062.2:n.1161-134_1161-133dup
NM_000265.5:c.1052-134_1052-133dup	NP_000256.4:n.1052-134_1052-133dup
XM_005250543.3:c.1014-134_1014-133dup	XP_005250600.2:n.1014-134_1014-133dup
XM_011516498.1:c.1051-134_1051-133dup	XP_011514800.1:n.1051-134_1051-133dup
XM_011516501.1:c.659-134_659-133dup	XP_011514803.1:n.659-134_659-133dup
NM_000265.6:c.1052-134_1052-133dup	NP_000256.4:n.1052-134_1052-133dup
NM_000265.7:c.1052-134_1052-133dup MANE Select	NP_000256.4:n.1052-134_1052-133dup