Canonical Allele Identifier: CA2466722931

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531506G= , CM000685.2:g.154531506G=	GRCh38
NC_000023.10:g.153759721G= , CM000685.1:g.153759721G=	GRCh37
NC_000023.9:g.153412915G=	NCBI36
NG_009015.2:g.21067C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.*494C=	ENSP00000377194.2:n.*494C=
ENST00000439227.6:c.*494C=	ENSP00000395599.2:n.*494C=
ENST00000696420.1:c.1457+682C=	ENSP00000512615.1:n.1457+682C=
ENST00000696421.1:c.1457+682C=	ENSP00000512616.1:n.1457+682C=
ENST00000696422.1:c.1905C=
ENST00000696423.1:c.1908C=
ENST00000696424.1:c.1894C=	ENSP00000512619.1:n.1894C=
ENST00000696425.1:c.*955C=	ENSP00000512620.1:n.*955C=
ENST00000696426.1:c.*1502C=	ENSP00000512621.1:n.*1502C=
ENST00000696427.1:c.*1002C=	ENSP00000512622.1:n.*1002C=
ENST00000696428.1:c.*1884C=	ENSP00000512623.1:n.*1884C=
ENST00000696429.1:c.*494C=	ENSP00000512624.1:n.*494C=
ENST00000696430.1:c.*494C=	ENSP00000512625.1:n.*494C=
ENST00000393562.10:c.*494C= MANE Select	ENSP00000377192.3:n.*494C=
ENST00000393562.6:c.*494C=	ENSP00000377192.2:n.*494C=
ENST00000621232.4:c.*494C=	ENSP00000483686.1:n.*494C=
NM_000402.4:c.*494C=	NP_000393.4:n.*494C=
NM_001042351.2:c.*494C=	NP_001035810.1:n.*494C=
XM_005274657.2:c.*494C=	XP_005274714.1:n.*494C=
XM_005274658.2:c.*494C=	XP_005274715.1:n.*494C=
NM_001360016.2:c.*494C= MANE Select	NP_001346945.1:n.*494C=
NM_001042351.3:c.*494C=	NP_001035810.1:n.*494C=