Canonical Allele Identifier: CA1717693201
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789218A= , CM000669.2:g.74789218A= GRCh38
NC_000007.13:g.74203562A= , CM000669.1:g.74203562A= GRCh37
NC_000007.12:g.73841498A= NCBI36
NG_009078.2:g.20255A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.*58A= MANE Select ENSP00000289473.4:n.*58A=
ENST00000289473.10:c.*58A= ENSP00000289473.4:n.*58A=
ENST00000289473.8:c.*58A= ENSP00000289473.4:n.*58A=
ENST00000398421.6:n.2258A=
ENST00000455062.2:n.1340A=
NM_000265.5:c.*58A= NP_000256.4:n.*58A=
XM_005250543.3:c.*152A= XP_005250600.2:n.*152A=
XM_011516498.1:c.*105A= XP_011514800.1:n.*105A=
XM_011516501.1:c.*58A= XP_011514803.1:n.*58A=
NM_000265.6:c.*58A= NP_000256.4:n.*58A=
NM_000265.7:c.*58A= MANE Select NP_000256.4:n.*58A=