Canonical Allele Identifier: CA2466722991

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531650C= , CM000685.2:g.154531650C=	GRCh38
NC_000023.10:g.153759865C= , CM000685.1:g.153759865C=	GRCh37
NC_000023.9:g.153413059C=	NCBI36
NG_009015.2:g.20923G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.*350G=	ENSP00000377194.2:n.*350G=
ENST00000439227.6:c.*350G=	ENSP00000395599.2:n.*350G=
ENST00000696420.1:c.1457+538G=	ENSP00000512615.1:n.1457+538G=
ENST00000696421.1:c.1457+538G=	ENSP00000512616.1:n.1457+538G=
ENST00000696422.1:c.1761G=
ENST00000696423.1:c.1764G=
ENST00000696424.1:c.1750G=	ENSP00000512619.1:n.1750G=
ENST00000696425.1:c.*811G=	ENSP00000512620.1:n.*811G=
ENST00000696426.1:c.*1358G=	ENSP00000512621.1:n.*1358G=
ENST00000696427.1:c.*858G=	ENSP00000512622.1:n.*858G=
ENST00000696428.1:c.*1740G=	ENSP00000512623.1:n.*1740G=
ENST00000696429.1:c.*350G=	ENSP00000512624.1:n.*350G=
ENST00000696430.1:c.*350G=	ENSP00000512625.1:n.*350G=
ENST00000393562.10:c.*350G= MANE Select	ENSP00000377192.3:n.*350G=
ENST00000393562.6:c.*350G=	ENSP00000377192.2:n.*350G=
ENST00000621232.4:c.*350G=	ENSP00000483686.1:n.*350G=
NM_000402.4:c.*350G=	NP_000393.4:n.*350G=
NM_001042351.2:c.*350G=	NP_001035810.1:n.*350G=
XM_005274657.2:c.*350G=	XP_005274714.1:n.*350G=
XM_005274658.2:c.*350G=	XP_005274715.1:n.*350G=
NM_001360016.2:c.*350G= MANE Select	NP_001346945.1:n.*350G=
NM_001042351.3:c.*350G=	NP_001035810.1:n.*350G=