Canonical Allele Identifier: CA2824282207
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154533181_154533182del , CM000685.2:g.154533181_154533182del GRCh38
NC_000023.10:g.153761396_153761397del , CM000685.1:g.153761396_153761397del GRCh37
NC_000023.9:g.153414590_153414591del NCBI36
NG_009015.2:g.19391_19392del

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.865-54_865-53del ENSP00000377194.2:n.865-54_865-53del
ENST00000439227.6:c.868-54_868-53del ENSP00000395599.2:n.868-54_868-53del
ENST00000696420.1:c.865-54_865-53del ENSP00000512615.1:n.865-54_865-53del
ENST00000696421.1:c.865-54_865-53del ENSP00000512616.1:n.865-54_865-53del
ENST00000696422.1:c.728-54_728-53del
ENST00000696423.1:c.731-54_731-53del
ENST00000696424.1:c.717-54_717-53del ENSP00000512619.1:n.717-54_717-53del
ENST00000696425.1:c.865-380_865-379del ENSP00000512620.1:n.865-380_865-379del
ENST00000696426.1:c.*271_*272del ENSP00000512621.1:n.*271_*272del
ENST00000696427.1:c.872-54_872-53del ENSP00000512622.1:n.872-54_872-53del
ENST00000696428.1:c.*707-54_*707-53del ENSP00000512623.1:n.*707-54_*707-53del
ENST00000696429.1:c.865-54_865-53del ENSP00000512624.1:n.865-54_865-53del
ENST00000696430.1:c.865-54_865-53del ENSP00000512625.1:n.865-54_865-53del
ENST00000393562.10:c.865-54_865-53del MANE Select ENSP00000377192.3:n.865-54_865-53del
ENST00000369620.6:c.1003-54_1003-53del ENSP00000358633.2:n.1003-54_1003-53del
ENST00000393562.6:c.955-54_955-53del ENSP00000377192.2:n.955-54_955-53del
ENST00000393564.6:c.865-54_865-53del ENSP00000377194.2:n.865-54_865-53del
ENST00000439227.5:c.868-54_868-53del ENSP00000395599.1:n.868-54_868-53del
ENST00000440967.5:c.868-54_868-53del ENSP00000400648.1:n.868-54_868-53del
ENST00000621232.4:c.865-54_865-53del ENSP00000483686.1:n.865-54_865-53del
NM_000402.4:c.955-54_955-53del NP_000393.4:n.955-54_955-53del
NM_001042351.2:c.865-54_865-53del NP_001035810.1:n.865-54_865-53del
XM_005274657.2:c.958-54_958-53del XP_005274714.1:n.958-54_958-53del
XM_005274658.2:c.868-54_868-53del XP_005274715.1:n.868-54_868-53del
XM_011531132.1:c.958-380_958-379del XP_011529434.1:n.958-380_958-379del
NM_001360016.2:c.865-54_865-53del MANE Select NP_001346945.1:n.865-54_865-53del
NM_001042351.3:c.865-54_865-53del NP_001035810.1:n.865-54_865-53del