Canonical Allele Identifier: CA1717693220
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789254G= , CM000669.2:g.74789254G= GRCh38
NC_000007.13:g.74203598G= , CM000669.1:g.74203598G= GRCh37
NC_000007.12:g.73841534G= NCBI36
NG_009078.2:g.20291G=

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*94G= MANE Select ENSP00000289473.4:n.*94G=
ENST00000289473.10:c.*94G= ENSP00000289473.4:n.*94G=
ENST00000289473.8:c.*94G= ENSP00000289473.4:n.*94G=
ENST00000398421.6:n.2294G=
ENST00000455062.2:n.1376G=
NM_000265.5:c.*94G= NP_000256.4:n.*94G=
XM_005250543.3:c.*188G= XP_005250600.2:n.*188G=
XM_011516498.1:c.*141G= XP_011514800.1:n.*141G=
XM_011516501.1:c.*94G= XP_011514803.1:n.*94G=
NM_000265.6:c.*94G= NP_000256.4:n.*94G=
NM_000265.7:c.*94G= MANE Select NP_000256.4:n.*94G=