Canonical Allele Identifier: CA2466723856

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533666G= , CM000685.2:g.154533666G=	GRCh38
NC_000023.10:g.153761881G= , CM000685.1:g.153761881G=	GRCh37
NC_000023.9:g.153415075G=	NCBI36
NG_009015.2:g.18907C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.774C=	ENSP00000377194.2:p.Asp258=
ENST00000439227.6:c.777C=	ENSP00000395599.2:p.Asp259=
ENST00000696420.1:c.774C=	ENSP00000512615.1:p.Asp258=
ENST00000696421.1:c.774C=	ENSP00000512616.1:p.Asp258=
ENST00000696422.1:c.637C=
ENST00000696423.1:c.640C=
ENST00000696424.1:c.651-25C=	ENSP00000512619.1:n.651-25C=
ENST00000696425.1:c.774C=	ENSP00000512620.1:p.Asp258=
ENST00000696426.1:c.774C=	ENSP00000512621.1:p.Asp258=
ENST00000696427.1:c.774C=	ENSP00000512622.1:p.Asp258=
ENST00000696428.1:c.*616C=	ENSP00000512623.1:n.*616C=
ENST00000696429.1:c.774C=	ENSP00000512624.1:p.Asp258=
ENST00000696430.1:c.774C=	ENSP00000512625.1:p.Asp258=
ENST00000393562.10:c.774C= MANE Select	ENSP00000377192.3:p.Asp258=
ENST00000369620.6:c.912C=	ENSP00000358633.2:p.Asp304=
ENST00000393562.6:c.864C=	ENSP00000377192.2:p.Asp288=
ENST00000393564.6:c.774C=	ENSP00000377194.2:p.Asp258=
ENST00000439227.5:c.777C=	ENSP00000395599.1:p.Asp259=
ENST00000440967.5:c.777C=	ENSP00000400648.1:p.Asp259=
ENST00000489497.1:n.163C=
ENST00000621232.4:c.774C=	ENSP00000483686.1:p.Asp258=
NM_000402.4:c.864C=	NP_000393.4:p.Asp288=
NM_001042351.2:c.774C=	NP_001035810.1:p.Asp258=
XM_005274657.2:c.867C=	XP_005274714.1:p.Asp289=
XM_005274658.2:c.777C=	XP_005274715.1:p.Asp259=
XM_011531132.1:c.867C=	XP_011529434.1:p.Asp289=
NM_001360016.2:c.774C= MANE Select	NP_001346945.1:p.Asp258=
NM_001042351.3:c.774C=	NP_001035810.1:p.Asp258=