Canonical Allele Identifier: CA1717693236
Gene: NCF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789271C= , CM000669.2:g.74789271C= GRCh38
NC_000007.13:g.74203615C= , CM000669.1:g.74203615C= GRCh37
NC_000007.12:g.73841551C= NCBI36
NG_009078.2:g.20308C=

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*111C= MANE Select ENSP00000289473.4:n.*111C=
ENST00000289473.10:c.*111C= ENSP00000289473.4:n.*111C=
ENST00000289473.8:c.*111C= ENSP00000289473.4:n.*111C=
ENST00000398421.6:n.2311C=
ENST00000455062.2:n.1393C=
NM_000265.5:c.*111C= NP_000256.4:n.*111C=
XM_005250543.3:c.*205C= XP_005250600.2:n.*205C=
XM_011516498.1:c.*158C= XP_011514800.1:n.*158C=
XM_011516501.1:c.*111C= XP_011514803.1:n.*111C=
NM_000265.6:c.*111C= NP_000256.4:n.*111C=
NM_000265.7:c.*111C= MANE Select NP_000256.4:n.*111C=