Canonical Allele Identifier: CA2466723547

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532924C= , CM000685.2:g.154532924C=	GRCh38
NC_000023.10:g.153761139C= , CM000685.1:g.153761139C=	GRCh37
NC_000023.9:g.153414333C=	NCBI36
NG_009015.2:g.19649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1051+18G=	ENSP00000377194.2:n.1051+18G=
ENST00000439227.6:c.1054+18G=	ENSP00000395599.2:n.1054+18G=
ENST00000696420.1:c.1051+18G=	ENSP00000512615.1:n.1051+18G=
ENST00000696421.1:c.1051+18G=	ENSP00000512616.1:n.1051+18G=
ENST00000696422.1:c.914+18G=
ENST00000696423.1:c.917+18G=
ENST00000696424.1:c.903+18G=	ENSP00000512619.1:n.903+18G=
ENST00000696425.1:c.865-122G=	ENSP00000512620.1:n.865-122G=
ENST00000696426.1:c.*511+18G=	ENSP00000512621.1:n.*511+18G=
ENST00000696427.1:c.*11+18G=	ENSP00000512622.1:n.*11+18G=
ENST00000696428.1:c.*893+18G=	ENSP00000512623.1:n.*893+18G=
ENST00000696429.1:c.1051+18G=	ENSP00000512624.1:n.1051+18G=
ENST00000696430.1:c.1051+18G=	ENSP00000512625.1:n.1051+18G=
ENST00000393562.10:c.1051+18G= MANE Select	ENSP00000377192.3:n.1051+18G=
ENST00000369620.6:c.1189+18G=	ENSP00000358633.2:n.1189+18G=
ENST00000393562.6:c.1141+18G=	ENSP00000377192.2:n.1141+18G=
ENST00000393564.6:c.1051+18G=	ENSP00000377194.2:n.1051+18G=
ENST00000490651.1:n.151G=
ENST00000621232.4:c.1051+18G=	ENSP00000483686.1:n.1051+18G=
NM_000402.4:c.1141+18G=	NP_000393.4:n.1141+18G=
NM_001042351.2:c.1051+18G=	NP_001035810.1:n.1051+18G=
XM_005274657.2:c.1144+18G=	XP_005274714.1:n.1144+18G=
XM_005274658.2:c.1054+18G=	XP_005274715.1:n.1054+18G=
XM_011531132.1:c.958-122G=	XP_011529434.1:n.958-122G=
NM_001360016.2:c.1051+18G= MANE Select	NP_001346945.1:n.1051+18G=
NM_001042351.3:c.1051+18G=	NP_001035810.1:n.1051+18G=