Canonical Allele Identifier: CA2552580631
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154534396_154534401del , CM000685.2:g.154534396_154534401del GRCh38
NC_000023.10:g.153762611_153762616del , CM000685.1:g.153762611_153762616del GRCh37
NC_000023.9:g.153415805_153415810del NCBI36
NG_009015.2:g.18172_18177del

Transcript Alleles

HGVS Amino-acid change
ENST00000393564.7:c.581_586del ENSP00000377194.2:p.Asp194_Ile196delinsVa...
ENST00000439227.6:c.584_589del ENSP00000395599.2:p.Asp195_Ile197delinsVa...
ENST00000696420.1:c.581_586del ENSP00000512615.1:p.Asp194_Ile196delinsVa...
ENST00000696421.1:c.581_586del ENSP00000512616.1:p.Asp194_Ile196delinsVa...
ENST00000696422.1:c.444_449del
ENST00000696423.1:c.447_452del
ENST00000696424.1:c.461_466del ENSP00000512619.1:p.Asp154_Ile156delinsVa...
ENST00000696425.1:c.581_586del ENSP00000512620.1:p.Asp194_Ile196delinsVa...
ENST00000696426.1:c.581_586del ENSP00000512621.1:p.Asp194_Ile196delinsVa...
ENST00000696427.1:c.581_586del ENSP00000512622.1:p.Asp194_Ile196delinsVa...
ENST00000696428.1:c.*423_*428del ENSP00000512623.1:n.*423_*428del
ENST00000696429.1:c.581_586del ENSP00000512624.1:p.Asp194_Ile196delinsVa...
ENST00000696430.1:c.581_586del ENSP00000512625.1:p.Asp194_Ile196delinsVa...
ENST00000393562.10:c.581_586del MANE Select ENSP00000377192.3:p.Asp194_Ile196delinsVa...
ENST00000369620.6:c.581_586del ENSP00000358633.2:p.Asp194_Ile196delinsVa...
ENST00000393562.6:c.671_676del ENSP00000377192.2:p.Asp224_Ile226delinsVa...
ENST00000393564.6:c.581_586del ENSP00000377194.2:p.Asp194_Ile196delinsVa...
ENST00000433845.1:c.581_586del ENSP00000394690.1:p.Asp194_Ile196delinsVa...
ENST00000439227.5:c.584_589del ENSP00000395599.1:p.Asp195_Ile197delinsVa...
ENST00000440967.5:c.584_589del ENSP00000400648.1:p.Asp195_Ile197delinsVa...
ENST00000621232.4:c.581_586del ENSP00000483686.1:p.Asp194_Ile196delinsVa...
NM_000402.4:c.671_676del NP_000393.4:p.Asp224_Ile226delinsVal
NM_001042351.2:c.581_586del NP_001035810.1:p.Asp194_Ile196delinsVal
XM_005274657.2:c.674_679del XP_005274714.1:p.Asp225_Ile227delinsVal
XM_005274658.2:c.584_589del XP_005274715.1:p.Asp195_Ile197delinsVal
XM_011531132.1:c.674_679del XP_011529434.1:p.Asp225_Ile227delinsVal
NM_001360016.2:c.581_586del MANE Select NP_001346945.1:p.Asp194_Ile196delinsVal
NM_001042351.3:c.581_586del NP_001035810.1:p.Asp194_Ile196delinsVal