Canonical Allele Identifier: CA2695146957
Gene: G6PD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154534439_154534440del , CM000685.2:g.154534439_154534440del GRCh38
NC_000023.10:g.153762654_153762655del , CM000685.1:g.153762654_153762655del GRCh37
NC_000023.9:g.153415848_153415849del NCBI36
NG_009015.2:g.18133_18134del

Transcript Alleles

HGVS Amino-acid change
ENST00000393564.7:c.542_543del ENSP00000377194.2:p.Asp181AlafsTer12
ENST00000439227.6:c.545_546del ENSP00000395599.2:p.Asp182AlafsTer12
ENST00000696420.1:c.542_543del ENSP00000512615.1:p.Asp181AlafsTer12
ENST00000696421.1:c.542_543del ENSP00000512616.1:p.Asp181AlafsTer12
ENST00000696422.1:c.405_406del
ENST00000696423.1:c.408_409del
ENST00000696424.1:c.422_423del ENSP00000512619.1:p.Asp141AlafsTer12
ENST00000696425.1:c.542_543del ENSP00000512620.1:p.Asp181AlafsTer12
ENST00000696426.1:c.542_543del ENSP00000512621.1:p.Asp181AlafsTer12
ENST00000696427.1:c.542_543del ENSP00000512622.1:p.Asp181AlafsTer12
ENST00000696428.1:c.*384_*385del ENSP00000512623.1:n.*384_*385del
ENST00000696429.1:c.542_543del ENSP00000512624.1:p.Asp181AlafsTer12
ENST00000696430.1:c.542_543del ENSP00000512625.1:p.Asp181AlafsTer12
ENST00000393562.10:c.542_543del MANE Select ENSP00000377192.3:p.Asp181AlafsTer12
ENST00000369620.6:c.542_543del ENSP00000358633.2:p.Asp181AlafsTer12
ENST00000393562.6:c.632_633del ENSP00000377192.2:p.Asp211AlafsTer12
ENST00000393564.6:c.542_543del ENSP00000377194.2:p.Asp181AlafsTer12
ENST00000433845.1:c.542_543del ENSP00000394690.1:p.Asp181AlafsTer12
ENST00000439227.5:c.545_546del ENSP00000395599.1:p.Asp182AlafsTer12
ENST00000440967.5:c.545_546del ENSP00000400648.1:p.Asp182AlafsTer12
ENST00000621232.4:c.542_543del ENSP00000483686.1:p.Asp181AlafsTer12
NM_000402.4:c.632_633del NP_000393.4:p.Asp211AlafsTer12
NM_001042351.2:c.542_543del NP_001035810.1:p.Asp181AlafsTer12
XM_005274657.2:c.635_636del XP_005274714.1:p.Asp212AlafsTer12
XM_005274658.2:c.545_546del XP_005274715.1:p.Asp182AlafsTer12
XM_011531132.1:c.635_636del XP_011529434.1:p.Asp212AlafsTer12
NM_001360016.2:c.542_543del MANE Select NP_001346945.1:p.Asp181AlafsTer12
NM_001042351.3:c.542_543del NP_001035810.1:p.Asp181AlafsTer12