Canonical Allele Identifier: CA1717693153
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789172A= , CM000669.2:g.74789172A= GRCh38
NC_000007.13:g.74203516A= , CM000669.1:g.74203516A= GRCh37
NC_000007.12:g.73841452A= NCBI36
NG_009078.2:g.20209A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.*12A= MANE Select ENSP00000289473.4:n.*12A=
ENST00000289473.10:c.*12A= ENSP00000289473.4:n.*12A=
ENST00000289473.8:c.*12A= ENSP00000289473.4:n.*12A=
ENST00000398421.6:n.2212A=
ENST00000455062.2:n.1294A=
NM_000265.5:c.*12A= NP_000256.4:n.*12A=
XM_005250543.3:c.*106A= XP_005250600.2:n.*106A=
XM_011516498.1:c.*59A= XP_011514800.1:n.*59A=
XM_011516501.1:c.*12A= XP_011514803.1:n.*12A=
NM_000265.6:c.*12A= NP_000256.4:n.*12A=
NM_000265.7:c.*12A= MANE Select NP_000256.4:n.*12A=