Canonical Allele Identifier: CA1717692959
Gene: NCF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789026T= , CM000669.2:g.74789026T= GRCh38
NC_000007.13:g.74203370T= , CM000669.1:g.74203370T= GRCh37
NC_000007.12:g.73841306T= NCBI36
NG_009078.2:g.20063T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.1052-13T= MANE Select ENSP00000289473.4:n.1052-13T=
ENST00000289473.10:c.1052-13T= ENSP00000289473.4:n.1052-13T=
ENST00000289473.8:c.1052-13T= ENSP00000289473.4:n.1052-13T=
ENST00000398421.6:n.2079-13T=
ENST00000455062.2:n.1161-13T=
NM_000265.5:c.1052-13T= NP_000256.4:n.1052-13T=
XM_005250543.3:c.1014-13T= XP_005250600.2:n.1014-13T=
XM_011516498.1:c.1051-13T= XP_011514800.1:n.1051-13T=
XM_011516501.1:c.659-13T= XP_011514803.1:n.659-13T=
NM_000265.6:c.1052-13T= NP_000256.4:n.1052-13T=
NM_000265.7:c.1052-13T= MANE Select NP_000256.4:n.1052-13T=
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