Canonical Allele Identifier: CA2683317934
Gene: NCF1 HGNC NCBI

Linked Data

gnomAD v4: 7-74788996-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74788996T>A , CM000669.2:g.74788996T>A GRCh38
NG_009078.2:g.20033T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.1052-43T>A MANE Select ENSP00000289473.4:n.1052-43T>A
ENST00000289473.10:c.1052-43T>A ENSP00000289473.4:n.1052-43T>A
ENST00000289473.8:c.1052-43T>A ENSP00000289473.4:n.1052-43T>A
ENST00000398421.6:n.2079-43T>A
ENST00000455062.2:n.1161-43T>A
NM_000265.5:c.1052-43T>A NP_000256.4:n.1052-43T>A
XM_005250543.3:c.1014-43T>A XP_005250600.2:n.1014-43T>A
XM_011516498.1:c.1051-43T>A XP_011514800.1:n.1051-43T>A
XM_011516501.1:c.659-43T>A XP_011514803.1:n.659-43T>A
NM_000265.6:c.1052-43T>A NP_000256.4:n.1052-43T>A
NM_000265.7:c.1052-43T>A MANE Select NP_000256.4:n.1052-43T>A
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