Canonical Allele Identifier: CA2683318109

Gene: NCF1

Linked Data

• gnomAD v4: 7-74789306-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789306T>G , CM000669.2:g.74789306T>G	GRCh38
NC_000007.13:g.74203650T>G , CM000669.1:g.74203650T>G	GRCh37
NC_000007.12:g.73841586T>G	NCBI36
NG_009078.2:g.20343T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*146T>G MANE Select	ENSP00000289473.4:n.*146T>G
ENST00000289473.10:c.*146T>G	ENSP00000289473.4:n.*146T>G
ENST00000289473.8:c.*146T>G	ENSP00000289473.4:n.*146T>G
ENST00000398421.6:n.2346T>G
ENST00000455062.2:n.1428T>G
NM_000265.5:c.*146T>G	NP_000256.4:n.*146T>G
XM_005250543.3:c.*240T>G	XP_005250600.2:n.*240T>G
XM_011516498.1:c.*193T>G	XP_011514800.1:n.*193T>G
XM_011516501.1:c.*146T>G	XP_011514803.1:n.*146T>G
NM_000265.6:c.*146T>G	NP_000256.4:n.*146T>G
NM_000265.7:c.*146T>G MANE Select	NP_000256.4:n.*146T>G