Canonical Allele Identifier: CA2466723417

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532581C= , CM000685.2:g.154532581C=	GRCh38
NC_000023.10:g.153760796C= , CM000685.1:g.153760796C=	GRCh37
NC_000023.9:g.153413990C=	NCBI36
NG_009015.2:g.19992G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1273G=	ENSP00000377194.2:p.Gly425=
ENST00000439227.6:c.1276G=	ENSP00000395599.2:p.Gly426=
ENST00000696420.1:c.1273G=	ENSP00000512615.1:p.Gly425=
ENST00000696421.1:c.1273G=	ENSP00000512616.1:p.Gly425=
ENST00000696422.1:c.1136G=
ENST00000696423.1:c.1139G=
ENST00000696424.1:c.1125G=	ENSP00000512619.1:n.1125G=
ENST00000696425.1:c.*186G=	ENSP00000512620.1:n.*186G=
ENST00000696426.1:c.*733G=	ENSP00000512621.1:n.*733G=
ENST00000696427.1:c.*233G=	ENSP00000512622.1:n.*233G=
ENST00000696428.1:c.*1115G=	ENSP00000512623.1:n.*1115G=
ENST00000696429.1:c.1273G=	ENSP00000512624.1:p.Gly425=
ENST00000696430.1:c.1273G=	ENSP00000512625.1:p.Gly425=
ENST00000393562.10:c.1273G= MANE Select	ENSP00000377192.3:p.Gly425=
ENST00000369620.6:c.1411G=	ENSP00000358633.2:p.Gly471=
ENST00000393562.6:c.1363G=	ENSP00000377192.2:p.Gly455=
ENST00000393564.6:c.1273G=	ENSP00000377194.2:p.Gly425=
ENST00000490651.1:n.494G=
ENST00000621232.4:c.1273G=	ENSP00000483686.1:p.Gly425=
NM_000402.4:c.1363G=	NP_000393.4:p.Gly455=
NM_001042351.2:c.1273G=	NP_001035810.1:p.Gly425=
XM_005274657.2:c.1366G=	XP_005274714.1:p.Gly456=
XM_005274658.2:c.1276G=	XP_005274715.1:p.Gly426=
XM_011531132.1:c.*186G=	XP_011529434.1:n.*186G=
NM_001360016.2:c.1273G= MANE Select	NP_001346945.1:p.Gly425=
NM_001042351.3:c.1273G=	NP_001035810.1:p.Gly425=