Canonical Allele Identifier: CA2466723584

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533002C= , CM000685.2:g.154533002C=	GRCh38
NC_000023.10:g.153761217C= , CM000685.1:g.153761217C=	GRCh37
NC_000023.9:g.153414411C=	NCBI36
NG_009015.2:g.19571G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.991G=	ENSP00000377194.2:p.Gly331=
ENST00000439227.6:c.994G=	ENSP00000395599.2:p.Gly332=
ENST00000696420.1:c.991G=	ENSP00000512615.1:p.Gly331=
ENST00000696421.1:c.991G=	ENSP00000512616.1:p.Gly331=
ENST00000696422.1:c.854G=
ENST00000696423.1:c.857G=
ENST00000696424.1:c.843G=	ENSP00000512619.1:n.843G=
ENST00000696425.1:c.865-200G=	ENSP00000512620.1:n.865-200G=
ENST00000696426.1:c.*451G=	ENSP00000512621.1:n.*451G=
ENST00000696427.1:c.998G=	ENSP00000512622.1:p.Arg333=
ENST00000696428.1:c.*833G=	ENSP00000512623.1:n.*833G=
ENST00000696429.1:c.991G=	ENSP00000512624.1:p.Gly331=
ENST00000696430.1:c.991G=	ENSP00000512625.1:p.Gly331=
ENST00000393562.10:c.991G= MANE Select	ENSP00000377192.3:p.Gly331=
ENST00000369620.6:c.1129G=	ENSP00000358633.2:p.Gly377=
ENST00000393562.6:c.1081G=	ENSP00000377192.2:p.Gly361=
ENST00000393564.6:c.991G=	ENSP00000377194.2:p.Gly331=
ENST00000439227.5:c.994G=	ENSP00000395599.1:p.Gly332=
ENST00000490651.1:n.73G=
ENST00000621232.4:c.991G=	ENSP00000483686.1:p.Gly331=
NM_000402.4:c.1081G=	NP_000393.4:p.Gly361=
NM_001042351.2:c.991G=	NP_001035810.1:p.Gly331=
XM_005274657.2:c.1084G=	XP_005274714.1:p.Gly362=
XM_005274658.2:c.994G=	XP_005274715.1:p.Gly332=
XM_011531132.1:c.958-200G=	XP_011529434.1:n.958-200G=
NM_001360016.2:c.991G= MANE Select	NP_001346945.1:p.Gly331=
NM_001042351.3:c.991G=	NP_001035810.1:p.Gly331=