Canonical Allele Identifier: CA1717693218
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789251A= , CM000669.2:g.74789251A= GRCh38
NC_000007.13:g.74203595A= , CM000669.1:g.74203595A= GRCh37
NC_000007.12:g.73841531A= NCBI36
NG_009078.2:g.20288A=

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*91A= MANE Select ENSP00000289473.4:n.*91A=
ENST00000289473.10:c.*91A= ENSP00000289473.4:n.*91A=
ENST00000289473.8:c.*91A= ENSP00000289473.4:n.*91A=
ENST00000398421.6:n.2291A=
ENST00000455062.2:n.1373A=
NM_000265.5:c.*91A= NP_000256.4:n.*91A=
XM_005250543.3:c.*185A= XP_005250600.2:n.*185A=
XM_011516498.1:c.*138A= XP_011514800.1:n.*138A=
XM_011516501.1:c.*91A= XP_011514803.1:n.*91A=
NM_000265.6:c.*91A= NP_000256.4:n.*91A=
NM_000265.7:c.*91A= MANE Select NP_000256.4:n.*91A=