Canonical Allele Identifier: CA1717693199
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789217T= , CM000669.2:g.74789217T= GRCh38
NC_000007.13:g.74203561T= , CM000669.1:g.74203561T= GRCh37
NC_000007.12:g.73841497T= NCBI36
NG_009078.2:g.20254T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.*57T= MANE Select ENSP00000289473.4:n.*57T=
ENST00000289473.10:c.*57T= ENSP00000289473.4:n.*57T=
ENST00000289473.8:c.*57T= ENSP00000289473.4:n.*57T=
ENST00000398421.6:n.2257T=
ENST00000455062.2:n.1339T=
NM_000265.5:c.*57T= NP_000256.4:n.*57T=
XM_005250543.3:c.*151T= XP_005250600.2:n.*151T=
XM_011516498.1:c.*104T= XP_011514800.1:n.*104T=
XM_011516501.1:c.*57T= XP_011514803.1:n.*57T=
NM_000265.6:c.*57T= NP_000256.4:n.*57T=
NM_000265.7:c.*57T= MANE Select NP_000256.4:n.*57T=