Canonical Allele Identifier: CA2466723482

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532784C= , CM000685.2:g.154532784C=	GRCh38
NC_000023.10:g.153760999C= , CM000685.1:g.153760999C=	GRCh37
NC_000023.9:g.153414193C=	NCBI36
NG_009015.2:g.19789G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1070G=	ENSP00000377194.2:p.Arg357=
ENST00000439227.6:c.1073G=	ENSP00000395599.2:p.Arg358=
ENST00000696420.1:c.1070G=	ENSP00000512615.1:p.Arg357=
ENST00000696421.1:c.1070G=	ENSP00000512616.1:p.Arg357=
ENST00000696422.1:c.933G=
ENST00000696423.1:c.936G=
ENST00000696424.1:c.922G=	ENSP00000512619.1:n.922G=
ENST00000696425.1:c.883G=	ENSP00000512620.1:p.Ala295=
ENST00000696426.1:c.*530G=	ENSP00000512621.1:n.*530G=
ENST00000696427.1:c.*30G=	ENSP00000512622.1:n.*30G=
ENST00000696428.1:c.*912G=	ENSP00000512623.1:n.*912G=
ENST00000696429.1:c.1070G=	ENSP00000512624.1:p.Arg357=
ENST00000696430.1:c.1070G=	ENSP00000512625.1:p.Arg357=
ENST00000393562.10:c.1070G= MANE Select	ENSP00000377192.3:p.Arg357=
ENST00000369620.6:c.1208G=	ENSP00000358633.2:p.Arg403=
ENST00000393562.6:c.1160G=	ENSP00000377192.2:p.Arg387=
ENST00000393564.6:c.1070G=	ENSP00000377194.2:p.Arg357=
ENST00000490651.1:n.291G=
ENST00000621232.4:c.1070G=	ENSP00000483686.1:p.Arg357=
NM_000402.4:c.1160G=	NP_000393.4:p.Arg387=
NM_001042351.2:c.1070G=	NP_001035810.1:p.Arg357=
XM_005274657.2:c.1163G=	XP_005274714.1:p.Arg388=
XM_005274658.2:c.1073G=	XP_005274715.1:p.Arg358=
XM_011531132.1:c.976G=	XP_011529434.1:p.Ala326=
NM_001360016.2:c.1070G= MANE Select	NP_001346945.1:p.Arg357=
NM_001042351.3:c.1070G=	NP_001035810.1:p.Arg357=