Canonical Allele Identifier: CA1717693228
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789261C= , CM000669.2:g.74789261C= GRCh38
NC_000007.13:g.74203605C= , CM000669.1:g.74203605C= GRCh37
NC_000007.12:g.73841541C= NCBI36
NG_009078.2:g.20298C=

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*101C= MANE Select ENSP00000289473.4:n.*101C=
ENST00000289473.10:c.*101C= ENSP00000289473.4:n.*101C=
ENST00000289473.8:c.*101C= ENSP00000289473.4:n.*101C=
ENST00000398421.6:n.2301C=
ENST00000455062.2:n.1383C=
NM_000265.5:c.*101C= NP_000256.4:n.*101C=
XM_005250543.3:c.*195C= XP_005250600.2:n.*195C=
XM_011516498.1:c.*148C= XP_011514800.1:n.*148C=
XM_011516501.1:c.*101C= XP_011514803.1:n.*101C=
NM_000265.6:c.*101C= NP_000256.4:n.*101C=
NM_000265.7:c.*101C= MANE Select NP_000256.4:n.*101C=