Canonical Allele Identifier: CA1103162905
Gene: NCF1 HGNC NCBI

Linked Data

gnomAD v3: 7-74789221-T-G
gnomAD v4: 7-74789221-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789221T>G , CM000669.2:g.74789221T>G GRCh38
NC_000007.13:g.74203565T>G , CM000669.1:g.74203565T>G GRCh37
NC_000007.12:g.73841501T>G NCBI36
NG_009078.2:g.20258T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.*61T>G MANE Select ENSP00000289473.4:n.*61T>G
ENST00000289473.10:c.*61T>G ENSP00000289473.4:n.*61T>G
ENST00000289473.8:c.*61T>G ENSP00000289473.4:n.*61T>G
ENST00000398421.6:n.2261T>G
ENST00000455062.2:n.1343T>G
NM_000265.5:c.*61T>G NP_000256.4:n.*61T>G
XM_005250543.3:c.*155T>G XP_005250600.2:n.*155T>G
XM_011516498.1:c.*108T>G XP_011514800.1:n.*108T>G
XM_011516501.1:c.*61T>G XP_011514803.1:n.*61T>G
NM_000265.6:c.*61T>G NP_000256.4:n.*61T>G
NM_000265.7:c.*61T>G MANE Select NP_000256.4:n.*61T>G