Canonical Allele Identifier: CA2466723359

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532461T= , CM000685.2:g.154532461T=	GRCh38
NC_000023.10:g.153760676T= , CM000685.1:g.153760676T=	GRCh37
NC_000023.9:g.153413870T=	NCBI36
NG_009015.2:g.20112A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1289A=	ENSP00000377194.2:p.Asn430=
ENST00000439227.6:c.1292A=	ENSP00000395599.2:p.Asn431=
ENST00000696420.1:c.1289A=	ENSP00000512615.1:p.Asn430=
ENST00000696421.1:c.1289A=	ENSP00000512616.1:p.Asn430=
ENST00000696422.1:c.1152A=
ENST00000696423.1:c.1155A=
ENST00000696424.1:c.1141A=	ENSP00000512619.1:n.1141A=
ENST00000696425.1:c.*202A=	ENSP00000512620.1:n.*202A=
ENST00000696426.1:c.*749A=	ENSP00000512621.1:n.*749A=
ENST00000696427.1:c.*249A=	ENSP00000512622.1:n.*249A=
ENST00000696428.1:c.*1131A=	ENSP00000512623.1:n.*1131A=
ENST00000696429.1:c.1289A=	ENSP00000512624.1:p.Asn430=
ENST00000696430.1:c.1289A=	ENSP00000512625.1:p.Asn430=
ENST00000393562.10:c.1289A= MANE Select	ENSP00000377192.3:p.Asn430=
ENST00000369620.6:c.1427A=	ENSP00000358633.2:p.Asn476=
ENST00000393562.6:c.1379A=	ENSP00000377192.2:p.Asn460=
ENST00000393564.6:c.1289A=	ENSP00000377194.2:p.Asn430=
ENST00000490651.1:n.510A=
ENST00000621232.4:c.1289A=	ENSP00000483686.1:p.Asn430=
NM_000402.4:c.1379A=	NP_000393.4:p.Asn460=
NM_001042351.2:c.1289A=	NP_001035810.1:p.Asn430=
XM_005274657.2:c.1382A=	XP_005274714.1:p.Asn461=
XM_005274658.2:c.1292A=	XP_005274715.1:p.Asn431=
NM_001360016.2:c.1289A= MANE Select	NP_001346945.1:p.Asn430=
NM_001042351.3:c.1289A=	NP_001035810.1:p.Asn430=