Canonical Allele Identifier: CA2824282545

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154534404_154534406del , CM000685.2:g.154534404_154534406del	GRCh38
NC_000023.10:g.153762619_153762621del , CM000685.1:g.153762619_153762621del	GRCh37
NC_000023.9:g.153415813_153415815del	NCBI36
NG_009015.2:g.18167_18169del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.576_578del	ENSP00000377194.2:p.Glu193del
ENST00000439227.6:c.579_581del	ENSP00000395599.2:p.Glu194del
ENST00000696420.1:c.576_578del	ENSP00000512615.1:p.Glu193del
ENST00000696421.1:c.576_578del	ENSP00000512616.1:p.Glu193del
ENST00000696422.1:c.439_441del
ENST00000696423.1:c.442_444del
ENST00000696424.1:c.456_458del	ENSP00000512619.1:p.Glu153del
ENST00000696425.1:c.576_578del	ENSP00000512620.1:p.Glu193del
ENST00000696426.1:c.576_578del	ENSP00000512621.1:p.Glu193del
ENST00000696427.1:c.576_578del	ENSP00000512622.1:p.Glu193del
ENST00000696428.1:c.*418_*420del	ENSP00000512623.1:n.*418_*420del
ENST00000696429.1:c.576_578del	ENSP00000512624.1:p.Glu193del
ENST00000696430.1:c.576_578del	ENSP00000512625.1:p.Glu193del
ENST00000393562.10:c.576_578del MANE Select	ENSP00000377192.3:p.Glu193del
ENST00000369620.6:c.576_578del	ENSP00000358633.2:p.Glu193del
ENST00000393562.6:c.666_668del	ENSP00000377192.2:p.Glu223del
ENST00000393564.6:c.576_578del	ENSP00000377194.2:p.Glu193del
ENST00000433845.1:c.576_578del	ENSP00000394690.1:p.Glu193del
ENST00000439227.5:c.579_581del	ENSP00000395599.1:p.Glu194del
ENST00000440967.5:c.579_581del	ENSP00000400648.1:p.Glu194del
ENST00000621232.4:c.576_578del	ENSP00000483686.1:p.Glu193del
NM_000402.4:c.666_668del	NP_000393.4:p.Glu223del
NM_001042351.2:c.576_578del	NP_001035810.1:p.Glu193del
XM_005274657.2:c.669_671del	XP_005274714.1:p.Glu224del
XM_005274658.2:c.579_581del	XP_005274715.1:p.Glu194del
XM_011531132.1:c.669_671del	XP_011529434.1:p.Glu224del
NM_001360016.2:c.576_578del MANE Select	NP_001346945.1:p.Glu193del
NM_001042351.3:c.576_578del	NP_001035810.1:p.Glu193del