Canonical Allele Identifier: CA2466722919

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531466A= , CM000685.2:g.154531466A=	GRCh38
NC_000023.10:g.153759681A= , CM000685.1:g.153759681A=	GRCh37
NC_000023.9:g.153412875A=	NCBI36
NG_009015.2:g.21107T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.*534T=	ENSP00000377194.2:n.*534T=
ENST00000439227.6:c.*534T=	ENSP00000395599.2:n.*534T=
ENST00000696420.1:c.1457+722T=	ENSP00000512615.1:n.1457+722T=
ENST00000696421.1:c.1457+722T=	ENSP00000512616.1:n.1457+722T=
ENST00000696422.1:c.1945T=
ENST00000696423.1:c.1948T=
ENST00000696424.1:c.1934T=	ENSP00000512619.1:n.1934T=
ENST00000696425.1:c.*995T=	ENSP00000512620.1:n.*995T=
ENST00000696426.1:c.*1542T=	ENSP00000512621.1:n.*1542T=
ENST00000696427.1:c.*1042T=	ENSP00000512622.1:n.*1042T=
ENST00000696428.1:c.*1924T=	ENSP00000512623.1:n.*1924T=
ENST00000696429.1:c.*534T=	ENSP00000512624.1:n.*534T=
ENST00000696430.1:c.*534T=	ENSP00000512625.1:n.*534T=
ENST00000393562.10:c.*534T= MANE Select	ENSP00000377192.3:n.*534T=
ENST00000393562.6:c.*534T=	ENSP00000377192.2:n.*534T=
ENST00000621232.4:c.*534T=	ENSP00000483686.1:n.*534T=
NM_000402.4:c.*534T=	NP_000393.4:n.*534T=
NM_001042351.2:c.*534T=	NP_001035810.1:n.*534T=
XM_005274657.2:c.*534T=	XP_005274714.1:n.*534T=
XM_005274658.2:c.*534T=	XP_005274715.1:n.*534T=
NM_001360016.2:c.*534T= MANE Select	NP_001346945.1:n.*534T=
NM_001042351.3:c.*534T=	NP_001035810.1:n.*534T=