Canonical Allele Identifier: CA1717693262
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789315_74789316delinsAC , CM000669.2:g.74789315_74789316delinsAC GRCh38
NC_000007.13:g.74203659_74203660delinsAC , CM000669.1:g.74203659_74203660delinsAC GRCh37
NC_000007.12:g.73841595_73841596delinsAC NCBI36
NG_009078.2:g.20352_20353delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.10:c.*155_*156delinsAC ENSP00000289473.4:n.*155_*156delinsAC
NM_000265.5:c.*155_*156delinsAC NP_000256.4:n.*155_*156delinsAC
XM_005250543.3:c.*249_*250delinsAC XP_005250600.2:n.*249_*250delinsAC
XM_011516498.1:c.*202_*203delinsAC XP_011514800.1:n.*202_*203delinsAC
XM_011516501.1:c.*155_*156delinsAC XP_011514803.1:n.*155_*156delinsAC
NM_000265.6:c.*155_*156delinsAC NP_000256.4:n.*155_*156delinsAC