Canonical Allele Identifier: CA1717693223
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789259C= , CM000669.2:g.74789259C= GRCh38
NC_000007.13:g.74203603C= , CM000669.1:g.74203603C= GRCh37
NC_000007.12:g.73841539C= NCBI36
NG_009078.2:g.20296C=

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*99C= MANE Select ENSP00000289473.4:n.*99C=
ENST00000289473.10:c.*99C= ENSP00000289473.4:n.*99C=
ENST00000289473.8:c.*99C= ENSP00000289473.4:n.*99C=
ENST00000398421.6:n.2299C=
ENST00000455062.2:n.1381C=
NM_000265.5:c.*99C= NP_000256.4:n.*99C=
XM_005250543.3:c.*193C= XP_005250600.2:n.*193C=
XM_011516498.1:c.*146C= XP_011514800.1:n.*146C=
XM_011516501.1:c.*99C= XP_011514803.1:n.*99C=
NM_000265.6:c.*99C= NP_000256.4:n.*99C=
NM_000265.7:c.*99C= MANE Select NP_000256.4:n.*99C=