Canonical Allele Identifier: CA2740130093

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532435G= , CM000685.2:g.154532435G=	GRCh38
NC_000023.10:g.153760650G= , CM000685.1:g.153760650G=	GRCh37
NC_000023.9:g.153413844G=	NCBI36
NG_009015.2:g.20138C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1315C=	ENSP00000377194.2:p.Arg439=
ENST00000439227.6:c.1318C=	ENSP00000395599.2:p.Arg440=
ENST00000696420.1:c.1315C=	ENSP00000512615.1:p.Arg439=
ENST00000696421.1:c.1315C=	ENSP00000512616.1:p.Arg439=
ENST00000696422.1:c.1178C=
ENST00000696423.1:c.1181C=
ENST00000696424.1:c.1167C=	ENSP00000512619.1:n.1167C=
ENST00000696425.1:c.*228C=	ENSP00000512620.1:n.*228C=
ENST00000696426.1:c.*775C=	ENSP00000512621.1:n.*775C=
ENST00000696427.1:c.*275C=	ENSP00000512622.1:n.*275C=
ENST00000696428.1:c.*1157C=	ENSP00000512623.1:n.*1157C=
ENST00000696429.1:c.1315C=	ENSP00000512624.1:p.Arg439=
ENST00000696430.1:c.1315C=	ENSP00000512625.1:p.Arg439=
ENST00000393562.10:c.1315C= MANE Select	ENSP00000377192.3:p.Arg439=
ENST00000369620.6:c.1453C=	ENSP00000358633.2:p.Arg485=
ENST00000393562.6:c.1405C=	ENSP00000377192.2:p.Arg469=
ENST00000393564.6:c.1315C=	ENSP00000377194.2:p.Arg439=
ENST00000490651.1:n.536C=
ENST00000621232.4:c.1315C=	ENSP00000483686.1:p.Arg439=
NM_000402.4:c.1405C=	NP_000393.4:p.Arg469=
NM_001042351.2:c.1315C=	NP_001035810.1:p.Arg439=
XM_005274657.2:c.1408C=	XP_005274714.1:p.Arg470=
XM_005274658.2:c.1318C=	XP_005274715.1:p.Arg440=
NM_001360016.2:c.1315C= MANE Select	NP_001346945.1:p.Arg439=
NM_001042351.3:c.1315C=	NP_001035810.1:p.Arg439=