Canonical Allele Identifier: CA2776494900
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789368del , CM000669.2:g.74789368del GRCh38
NC_000007.13:g.74203712del , CM000669.1:g.74203712del GRCh37
NC_000007.12:g.73841648del NCBI36
NG_009078.2:g.20405del

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.10:c.*208del ENSP00000289473.4:n.*208del
NM_000265.5:c.*208del NP_000256.4:n.*208del
XM_005250543.3:c.*302del XP_005250600.2:n.*302del
XM_011516498.1:c.*255del XP_011514800.1:n.*255del
XM_011516501.1:c.*208del XP_011514803.1:n.*208del
NM_000265.6:c.*208del NP_000256.4:n.*208del