Canonical Allele Identifier: CA2683317984

Gene: NCF1

Linked Data

• gnomAD v4: 7-74789201-GCCCCGTGCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74789202_74789211del , CM000669.2:g.74789202_74789211del	GRCh38
NC_000007.13:g.74203546_74203555del , CM000669.1:g.74203546_74203555del	GRCh37
NC_000007.12:g.73841482_73841491del	NCBI36
NG_009078.2:g.20239_20248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.*42_*51del MANE Select	ENSP00000289473.4:n.*42_*51del
ENST00000289473.10:c.*42_*51del	ENSP00000289473.4:n.*42_*51del
ENST00000289473.8:c.*42_*51del	ENSP00000289473.4:n.*42_*51del
ENST00000398421.6:n.2242_2251del
ENST00000455062.2:n.1324_1333del
NM_000265.5:c.*42_*51del	NP_000256.4:n.*42_*51del
XM_005250543.3:c.*136_*145del	XP_005250600.2:n.*136_*145del
XM_011516498.1:c.*89_*98del	XP_011514800.1:n.*89_*98del
XM_011516501.1:c.*42_*51del	XP_011514803.1:n.*42_*51del
NM_000265.6:c.*42_*51del	NP_000256.4:n.*42_*51del
NM_000265.7:c.*42_*51del MANE Select	NP_000256.4:n.*42_*51del