Canonical Allele Identifier: CA1717692803
Gene: NCF1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74788946T= , CM000669.2:g.74788946T= GRCh38
NC_000007.13:g.74203290T= , CM000669.1:g.74203290T= GRCh37
NC_000007.12:g.73841226T= NCBI36
NG_009078.2:g.19983T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.1052-93T= MANE Select ENSP00000289473.4:n.1052-93T=
ENST00000289473.10:c.1052-93T= ENSP00000289473.4:n.1052-93T=
ENST00000289473.8:c.1052-93T= ENSP00000289473.4:n.1052-93T=
ENST00000398421.6:n.2079-93T=
ENST00000455062.2:n.1161-93T=
NM_000265.5:c.1052-93T= NP_000256.4:n.1052-93T=
XM_005250543.3:c.1014-93T= XP_005250600.2:n.1014-93T=
XM_011516498.1:c.1051-93T= XP_011514800.1:n.1051-93T=
XM_011516501.1:c.659-93T= XP_011514803.1:n.659-93T=
NM_000265.6:c.1052-93T= NP_000256.4:n.1052-93T=
NM_000265.7:c.1052-93T= MANE Select NP_000256.4:n.1052-93T=
Search 100 bp 5'
Search 100 bp 3'