Canonical Allele Identifier: CA2579741981
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154532111_154532113del , CM000685.2:g.154532111_154532113del GRCh38
NC_000023.10:g.153760326_153760328del , CM000685.1:g.153760326_153760328del GRCh37
NC_000023.9:g.153413520_153413522del NCBI36
NG_009015.2:g.20464_20466del

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.1458-19_1458-17del ENSP00000377194.2:n.1458-19_1458-17del
ENST00000439227.6:c.1461-19_1461-17del ENSP00000395599.2:n.1461-19_1461-17del
ENST00000696420.1:c.1457+79_1457+81del ENSP00000512615.1:n.1457+79_1457+81del
ENST00000696421.1:c.1457+79_1457+81del ENSP00000512616.1:n.1457+79_1457+81del
ENST00000696422.1:c.1321-19_1321-17del
ENST00000696423.1:c.1324-19_1324-17del
ENST00000696424.1:c.1310-19_1310-17del ENSP00000512619.1:n.1310-19_1310-17del
ENST00000696425.1:c.*371-19_*371-17del ENSP00000512620.1:n.*371-19_*371-17del
ENST00000696426.1:c.*918-19_*918-17del ENSP00000512621.1:n.*918-19_*918-17del
ENST00000696427.1:c.*418-19_*418-17del ENSP00000512622.1:n.*418-19_*418-17del
ENST00000696428.1:c.*1300-19_*1300-17del ENSP00000512623.1:n.*1300-19_*1300-17del
ENST00000696429.1:c.1458-19_1458-17del ENSP00000512624.1:n.1458-19_1458-17del
ENST00000696430.1:c.1458-19_1458-17del ENSP00000512625.1:n.1458-19_1458-17del
ENST00000393562.10:c.1458-19_1458-17del MANE Select ENSP00000377192.3:n.1458-19_1458-17del
ENST00000369620.6:c.1596-19_1596-17del ENSP00000358633.2:n.1596-19_1596-17del
ENST00000393562.6:c.1548-19_1548-17del ENSP00000377192.2:n.1548-19_1548-17del
ENST00000393564.6:c.1458-19_1458-17del ENSP00000377194.2:n.1458-19_1458-17del
ENST00000490651.1:n.757_759del
ENST00000621232.4:c.1458-19_1458-17del ENSP00000483686.1:n.1458-19_1458-17del
NM_000402.4:c.1548-19_1548-17del NP_000393.4:n.1548-19_1548-17del
NM_001042351.2:c.1458-19_1458-17del NP_001035810.1:n.1458-19_1458-17del
XM_005274657.2:c.1551-19_1551-17del XP_005274714.1:n.1551-19_1551-17del
XM_005274658.2:c.1461-19_1461-17del XP_005274715.1:n.1461-19_1461-17del
NM_001360016.2:c.1458-19_1458-17del MANE Select NP_001346945.1:n.1458-19_1458-17del
NM_001042351.3:c.1458-19_1458-17del NP_001035810.1:n.1458-19_1458-17del