Canonical Allele Identifier: CA2740130027

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532458A= , CM000685.2:g.154532458A=	GRCh38
NC_000023.10:g.153760673A= , CM000685.1:g.153760673A=	GRCh37
NC_000023.9:g.153413867A=	NCBI36
NG_009015.2:g.20115T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1292T=	ENSP00000377194.2:p.Val431=
ENST00000439227.6:c.1295T=	ENSP00000395599.2:p.Val432=
ENST00000696420.1:c.1292T=	ENSP00000512615.1:p.Val431=
ENST00000696421.1:c.1292T=	ENSP00000512616.1:p.Val431=
ENST00000696422.1:c.1155T=
ENST00000696423.1:c.1158T=
ENST00000696424.1:c.1144T=	ENSP00000512619.1:n.1144T=
ENST00000696425.1:c.*205T=	ENSP00000512620.1:n.*205T=
ENST00000696426.1:c.*752T=	ENSP00000512621.1:n.*752T=
ENST00000696427.1:c.*252T=	ENSP00000512622.1:n.*252T=
ENST00000696428.1:c.*1134T=	ENSP00000512623.1:n.*1134T=
ENST00000696429.1:c.1292T=	ENSP00000512624.1:p.Val431=
ENST00000696430.1:c.1292T=	ENSP00000512625.1:p.Val431=
ENST00000393562.10:c.1292T= MANE Select	ENSP00000377192.3:p.Val431=
ENST00000369620.6:c.1430T=	ENSP00000358633.2:p.Val477=
ENST00000393562.6:c.1382T=	ENSP00000377192.2:p.Val461=
ENST00000393564.6:c.1292T=	ENSP00000377194.2:p.Val431=
ENST00000490651.1:n.513T=
ENST00000621232.4:c.1292T=	ENSP00000483686.1:p.Val431=
NM_000402.4:c.1382T=	NP_000393.4:p.Val461=
NM_001042351.2:c.1292T=	NP_001035810.1:p.Val431=
XM_005274657.2:c.1385T=	XP_005274714.1:p.Val462=
XM_005274658.2:c.1295T=	XP_005274715.1:p.Val432=
NM_001360016.2:c.1292T= MANE Select	NP_001346945.1:p.Val431=
NM_001042351.3:c.1292T=	NP_001035810.1:p.Val431=