Canonical Allele Identifier: CA2683318093
Gene: NCF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789267_74789268del , CM000669.2:g.74789267_74789268del GRCh38
NC_000007.13:g.74203611_74203612del , CM000669.1:g.74203611_74203612del GRCh37
NC_000007.12:g.73841547_73841548del NCBI36
NG_009078.2:g.20304_20305del

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*107_*108del MANE Select ENSP00000289473.4:n.*107_*108del
ENST00000289473.10:c.*107_*108del ENSP00000289473.4:n.*107_*108del
ENST00000289473.8:c.*107_*108del ENSP00000289473.4:n.*107_*108del
ENST00000398421.6:n.2307_2308del
ENST00000455062.2:n.1389_1390del
NM_000265.5:c.*107_*108del NP_000256.4:n.*107_*108del
XM_005250543.3:c.*201_*202del XP_005250600.2:n.*201_*202del
XM_011516498.1:c.*154_*155del XP_011514800.1:n.*154_*155del
XM_011516501.1:c.*107_*108del XP_011514803.1:n.*107_*108del
NM_000265.6:c.*107_*108del NP_000256.4:n.*107_*108del
NM_000265.7:c.*107_*108del MANE Select NP_000256.4:n.*107_*108del