Canonical Allele Identifier: CA2683317957
Gene: NCF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74789044_74789046del , CM000669.2:g.74789044_74789046del GRCh38
NC_000007.13:g.74203388_74203390del , CM000669.1:g.74203388_74203390del GRCh37
NC_000007.12:g.73841324_73841326del NCBI36
NG_009078.2:g.20081_20083del

Transcript Alleles

HGVS Amino-acid Change
ENST00000289473.11:c.1057_1059del
ENST00000289473.10:c.1057_1059del
ENST00000289473.8:c.1057_1059del
ENST00000398421.6:n.2084_2086del
ENST00000455062.2:n.1166_1168del
NM_000265.5:c.1057_1059del
XM_005250543.3:c.1019_1021del
XM_011516498.1:c.1056_1058del
XM_011516501.1:c.664_666del
NM_000265.6:c.1057_1059del
NM_000265.7:c.1057_1059del