Canonical Allele Identifier: CA2466723357

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532459C= , CM000685.2:g.154532459C=	GRCh38
NC_000023.10:g.153760674C= , CM000685.1:g.153760674C=	GRCh37
NC_000023.9:g.153413868C=	NCBI36
NG_009015.2:g.20114G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1291G=	ENSP00000377194.2:p.Val431=
ENST00000439227.6:c.1294G=	ENSP00000395599.2:p.Val432=
ENST00000696420.1:c.1291G=	ENSP00000512615.1:p.Val431=
ENST00000696421.1:c.1291G=	ENSP00000512616.1:p.Val431=
ENST00000696422.1:c.1154G=
ENST00000696423.1:c.1157G=
ENST00000696424.1:c.1143G=	ENSP00000512619.1:n.1143G=
ENST00000696425.1:c.*204G=	ENSP00000512620.1:n.*204G=
ENST00000696426.1:c.*751G=	ENSP00000512621.1:n.*751G=
ENST00000696427.1:c.*251G=	ENSP00000512622.1:n.*251G=
ENST00000696428.1:c.*1133G=	ENSP00000512623.1:n.*1133G=
ENST00000696429.1:c.1291G=	ENSP00000512624.1:p.Val431=
ENST00000696430.1:c.1291G=	ENSP00000512625.1:p.Val431=
ENST00000393562.10:c.1291G= MANE Select	ENSP00000377192.3:p.Val431=
ENST00000369620.6:c.1429G=	ENSP00000358633.2:p.Val477=
ENST00000393562.6:c.1381G=	ENSP00000377192.2:p.Val461=
ENST00000393564.6:c.1291G=	ENSP00000377194.2:p.Val431=
ENST00000490651.1:n.512G=
ENST00000621232.4:c.1291G=	ENSP00000483686.1:p.Val431=
NM_000402.4:c.1381G=	NP_000393.4:p.Val461=
NM_001042351.2:c.1291G=	NP_001035810.1:p.Val431=
XM_005274657.2:c.1384G=	XP_005274714.1:p.Val462=
XM_005274658.2:c.1294G=	XP_005274715.1:p.Val432=
NM_001360016.2:c.1291G= MANE Select	NP_001346945.1:p.Val431=
NM_001042351.3:c.1291G=	NP_001035810.1:p.Val431=