Canonical Allele Identifier: CA367956123
Gene: NCF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.74203485A>G (hg19) chr7:g.74789141A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789141A>G , CM000669.2:g.74789141A>G GRCh38
NC_000007.13:g.74203485A>G , CM000669.1:g.74203485A>G GRCh37
NC_000007.12:g.73841421A>G NCBI36
NG_009078.2:g.20178A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.1154A>G MANE Select ENSP00000289473.4:p.Lys385Arg
ENST00000289473.10:c.1154A>G ENSP00000289473.4:p.Lys385Arg
ENST00000289473.8:c.1154A>G ENSP00000289473.4:p.Lys385Arg
ENST00000398421.6:n.2181A>G
ENST00000455062.2:n.1263A>G
NM_000265.5:c.1154A>G NP_000256.4:p.Lys385Arg
XM_005250543.3:c.*75A>G XP_005250600.2:n.*75A>G
XM_011516498.1:c.*28A>G XP_011514800.1:n.*28A>G
XM_011516501.1:c.761A>G XP_011514803.1:p.Lys254Arg
NM_000265.6:c.1154A>G NP_000256.4:p.Lys385Arg
NM_000265.7:c.1154A>G MANE Select NP_000256.4:p.Lys385Arg
Search 100 bp 5'
Search 100 bp 3'