Canonical Allele Identifier: CA2466723276

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532249T= , CM000685.2:g.154532249T=	GRCh38
NC_000023.10:g.153760464T= , CM000685.1:g.153760464T=	GRCh37
NC_000023.9:g.153413658T=	NCBI36
NG_009015.2:g.20324A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1396A=	ENSP00000377194.2:p.Thr466=
ENST00000439227.6:c.1399A=	ENSP00000395599.2:p.Thr467=
ENST00000696420.1:c.1396A=	ENSP00000512615.1:p.Thr466=
ENST00000696421.1:c.1396A=	ENSP00000512616.1:p.Thr466=
ENST00000696422.1:c.1259A=
ENST00000696423.1:c.1262A=
ENST00000696424.1:c.1248A=	ENSP00000512619.1:n.1248A=
ENST00000696425.1:c.*309A=	ENSP00000512620.1:n.*309A=
ENST00000696426.1:c.*856A=	ENSP00000512621.1:n.*856A=
ENST00000696427.1:c.*356A=	ENSP00000512622.1:n.*356A=
ENST00000696428.1:c.*1238A=	ENSP00000512623.1:n.*1238A=
ENST00000696429.1:c.1396A=	ENSP00000512624.1:p.Thr466=
ENST00000696430.1:c.1396A=	ENSP00000512625.1:p.Thr466=
ENST00000393562.10:c.1396A= MANE Select	ENSP00000377192.3:p.Thr466=
ENST00000369620.6:c.1534A=	ENSP00000358633.2:p.Thr512=
ENST00000393562.6:c.1486A=	ENSP00000377192.2:p.Thr496=
ENST00000393564.6:c.1396A=	ENSP00000377194.2:p.Thr466=
ENST00000490651.1:n.617A=
ENST00000621232.4:c.1396A=	ENSP00000483686.1:p.Thr466=
NM_000402.4:c.1486A=	NP_000393.4:p.Thr496=
NM_001042351.2:c.1396A=	NP_001035810.1:p.Thr466=
XM_005274657.2:c.1489A=	XP_005274714.1:p.Thr497=
XM_005274658.2:c.1399A=	XP_005274715.1:p.Thr467=
NM_001360016.2:c.1396A= MANE Select	NP_001346945.1:p.Thr466=
NM_001042351.3:c.1396A=	NP_001035810.1:p.Thr466=