Canonical Allele Identifier: CA2683318111

Gene: NCF1

Linked Data

• gnomAD v4: 7-74789312-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789312T>G , CM000669.2:g.74789312T>G	GRCh38
NC_000007.13:g.74203656T>G , CM000669.1:g.74203656T>G	GRCh37
NC_000007.12:g.73841592T>G	NCBI36
NG_009078.2:g.20349T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*152T>G MANE Select	ENSP00000289473.4:n.*152T>G
ENST00000289473.10:c.*152T>G	ENSP00000289473.4:n.*152T>G
ENST00000289473.8:c.*152T>G	ENSP00000289473.4:n.*152T>G
ENST00000398421.6:n.2352T>G
ENST00000455062.2:n.1434T>G
NM_000265.5:c.*152T>G	NP_000256.4:n.*152T>G
XM_005250543.3:c.*246T>G	XP_005250600.2:n.*246T>G
XM_011516498.1:c.*199T>G	XP_011514800.1:n.*199T>G
XM_011516501.1:c.*152T>G	XP_011514803.1:n.*152T>G
NM_000265.6:c.*152T>G	NP_000256.4:n.*152T>G
NM_000265.7:c.*152T>G MANE Select	NP_000256.4:n.*152T>G