Canonical Allele Identifier: CA2683317932

Gene: NCF1

Linked Data

• gnomAD v4: 7-74788994-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74788994_74788995insTG , CM000669.2:g.74788994_74788995insTG	GRCh38
NC_000007.13:g.74203338_74203339insTG , CM000669.1:g.74203338_74203339insTG	GRCh37
NC_000007.12:g.73841274_73841275insTG	NCBI36
NG_009078.2:g.20031_20032insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1052-45_1052-44insTG MANE Select	ENSP00000289473.4:n.1052-45_1052-44insTG
ENST00000289473.10:c.1052-45_1052-44insTG	ENSP00000289473.4:n.1052-45_1052-44insTG
ENST00000289473.8:c.1052-45_1052-44insTG	ENSP00000289473.4:n.1052-45_1052-44insTG
ENST00000398421.6:n.2079-45_2079-44insTG
ENST00000455062.2:n.1161-45_1161-44insTG
NM_000265.5:c.1052-45_1052-44insTG	NP_000256.4:n.1052-45_1052-44insTG
XM_005250543.3:c.1014-45_1014-44insTG	XP_005250600.2:n.1014-45_1014-44insTG
XM_011516498.1:c.1051-45_1051-44insTG	XP_011514800.1:n.1051-45_1051-44insTG
XM_011516501.1:c.659-45_659-44insTG	XP_011514803.1:n.659-45_659-44insTG
NM_000265.6:c.1052-45_1052-44insTG	NP_000256.4:n.1052-45_1052-44insTG
NM_000265.7:c.1052-45_1052-44insTG MANE Select	NP_000256.4:n.1052-45_1052-44insTG