Canonical Allele Identifier: CA1717692740

Gene: NCF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74788896_74788898delinsCAG , CM000669.2:g.74788896_74788898delinsCAG	GRCh38
NC_000007.13:g.74203240_74203242delinsCAG , CM000669.1:g.74203240_74203242delinsCAG	GRCh37
NC_000007.12:g.73841176_73841178delinsCAG	NCBI36
NG_009078.2:g.19933_19935delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.1052-143_1052-141delinsCAG MANE Select	ENSP00000289473.4:n.1052-143_1052-141delinsCAG
ENST00000289473.10:c.1052-143_1052-141delinsCAG	ENSP00000289473.4:n.1052-143_1052-141delinsCAG
ENST00000289473.8:c.1052-143_1052-141delinsCAG	ENSP00000289473.4:n.1052-143_1052-141delinsCAG
ENST00000398421.6:n.2079-143_2079-141delinsCAG
ENST00000455062.2:n.1161-143_1161-141delinsCAG
NM_000265.5:c.1052-143_1052-141delinsCAG	NP_000256.4:n.1052-143_1052-141delinsCAG
XM_005250543.3:c.1014-143_1014-141delinsCAG	XP_005250600.2:n.1014-143_1014-141delinsCAG
XM_011516498.1:c.1051-143_1051-141delinsCAG	XP_011514800.1:n.1051-143_1051-141delinsCAG
XM_011516501.1:c.659-143_659-141delinsCAG	XP_011514803.1:n.659-143_659-141delinsCAG
NM_000265.6:c.1052-143_1052-141delinsCAG	NP_000256.4:n.1052-143_1052-141delinsCAG
NM_000265.7:c.1052-143_1052-141delinsCAG MANE Select	NP_000256.4:n.1052-143_1052-141delinsCAG