Canonical Allele Identifier: CA2466723442

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532667G= , CM000685.2:g.154532667G=	GRCh38
NC_000023.10:g.153760882G= , CM000685.1:g.153760882G=	GRCh37
NC_000023.9:g.153414076G=	NCBI36
NG_009015.2:g.19906C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1187C=	ENSP00000377194.2:p.Pro396=
ENST00000439227.6:c.1190C=	ENSP00000395599.2:p.Pro397=
ENST00000696420.1:c.1187C=	ENSP00000512615.1:p.Pro396=
ENST00000696421.1:c.1187C=	ENSP00000512616.1:p.Pro396=
ENST00000696422.1:c.1050C=
ENST00000696423.1:c.1053C=
ENST00000696424.1:c.1039C=	ENSP00000512619.1:n.1039C=
ENST00000696425.1:c.*100C=	ENSP00000512620.1:n.*100C=
ENST00000696426.1:c.*647C=	ENSP00000512621.1:n.*647C=
ENST00000696427.1:c.*147C=	ENSP00000512622.1:n.*147C=
ENST00000696428.1:c.*1029C=	ENSP00000512623.1:n.*1029C=
ENST00000696429.1:c.1187C=	ENSP00000512624.1:p.Pro396=
ENST00000696430.1:c.1187C=	ENSP00000512625.1:p.Pro396=
ENST00000393562.10:c.1187C= MANE Select	ENSP00000377192.3:p.Pro396=
ENST00000369620.6:c.1325C=	ENSP00000358633.2:p.Pro442=
ENST00000393562.6:c.1277C=	ENSP00000377192.2:p.Pro426=
ENST00000393564.6:c.1187C=	ENSP00000377194.2:p.Pro396=
ENST00000490651.1:n.408C=
ENST00000621232.4:c.1187C=	ENSP00000483686.1:p.Pro396=
NM_000402.4:c.1277C=	NP_000393.4:p.Pro426=
NM_001042351.2:c.1187C=	NP_001035810.1:p.Pro396=
XM_005274657.2:c.1280C=	XP_005274714.1:p.Pro427=
XM_005274658.2:c.1190C=	XP_005274715.1:p.Pro397=
XM_011531132.1:c.*100C=	XP_011529434.1:n.*100C=
NM_001360016.2:c.1187C= MANE Select	NP_001346945.1:p.Pro396=
NM_001042351.3:c.1187C=	NP_001035810.1:p.Pro396=