Canonical Allele Identifier: CA1103162775
Gene: NCF1 HGNC NCBI

Linked Data

gnomAD v3: 7-74789191-G-A
gnomAD v4: 7-74789191-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789191G>A , CM000669.2:g.74789191G>A GRCh38
NC_000007.13:g.74203535G>A , CM000669.1:g.74203535G>A GRCh37
NC_000007.12:g.73841471G>A NCBI36
NG_009078.2:g.20228G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.*31G>A MANE Select ENSP00000289473.4:n.*31G>A
ENST00000289473.10:c.*31G>A ENSP00000289473.4:n.*31G>A
ENST00000289473.8:c.*31G>A ENSP00000289473.4:n.*31G>A
ENST00000398421.6:n.2231G>A
ENST00000455062.2:n.1313G>A
NM_000265.5:c.*31G>A NP_000256.4:n.*31G>A
XM_005250543.3:c.*125G>A XP_005250600.2:n.*125G>A
XM_011516498.1:c.*78G>A XP_011514800.1:n.*78G>A
XM_011516501.1:c.*31G>A XP_011514803.1:n.*31G>A
NM_000265.6:c.*31G>A NP_000256.4:n.*31G>A
NM_000265.7:c.*31G>A MANE Select NP_000256.4:n.*31G>A
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