Canonical Allele Identifier: CA2776494875
Gene: NCF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789179A>T , CM000669.2:g.74789179A>T GRCh38
NC_000007.13:g.74203523A>T , CM000669.1:g.74203523A>T GRCh37
NC_000007.12:g.73841459A>T NCBI36
NG_009078.2:g.20216A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000289473.11:c.*19A>T MANE Select ENSP00000289473.4:n.*19A>T
ENST00000289473.10:c.*19A>T ENSP00000289473.4:n.*19A>T
ENST00000289473.8:c.*19A>T ENSP00000289473.4:n.*19A>T
ENST00000398421.6:n.2219A>T
ENST00000455062.2:n.1301A>T
NM_000265.5:c.*19A>T NP_000256.4:n.*19A>T
XM_005250543.3:c.*113A>T XP_005250600.2:n.*113A>T
XM_011516498.1:c.*66A>T XP_011514800.1:n.*66A>T
XM_011516501.1:c.*19A>T XP_011514803.1:n.*19A>T
NM_000265.6:c.*19A>T NP_000256.4:n.*19A>T
NM_000265.7:c.*19A>T MANE Select NP_000256.4:n.*19A>T
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