Canonical Allele Identifier: CA2683318021
Gene: NCF1 HGNC NCBI

Linked Data

gnomAD v4: 7-74789220-G-GC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789220_74789221insC , CM000669.2:g.74789220_74789221insC GRCh38
NC_000007.13:g.74203564_74203565insC , CM000669.1:g.74203564_74203565insC GRCh37
NC_000007.12:g.73841500_73841501insC NCBI36
NG_009078.2:g.20257_20258insC

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*60_*61insC MANE Select ENSP00000289473.4:n.*60_*61insC
ENST00000289473.10:c.*60_*61insC ENSP00000289473.4:n.*60_*61insC
ENST00000289473.8:c.*60_*61insC ENSP00000289473.4:n.*60_*61insC
ENST00000398421.6:n.2260_2261insC
ENST00000455062.2:n.1342_1343insC
NM_000265.5:c.*60_*61insC NP_000256.4:n.*60_*61insC
XM_005250543.3:c.*154_*155insC XP_005250600.2:n.*154_*155insC
XM_011516498.1:c.*107_*108insC XP_011514800.1:n.*107_*108insC
XM_011516501.1:c.*60_*61insC XP_011514803.1:n.*60_*61insC
NM_000265.6:c.*60_*61insC NP_000256.4:n.*60_*61insC
NM_000265.7:c.*60_*61insC MANE Select NP_000256.4:n.*60_*61insC
Search 100 bp 5'
Search 100 bp 3'