Canonical Allele Identifier: CA2740130043

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532987T= , CM000685.2:g.154532987T=	GRCh38
NC_000023.10:g.153761202T= , CM000685.1:g.153761202T=	GRCh37
NC_000023.9:g.153414396T=	NCBI36
NG_009015.2:g.19586A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1006A=	ENSP00000377194.2:p.Thr336=
ENST00000439227.6:c.1009A=	ENSP00000395599.2:p.Thr337=
ENST00000696420.1:c.1006A=	ENSP00000512615.1:p.Thr336=
ENST00000696421.1:c.1006A=	ENSP00000512616.1:p.Thr336=
ENST00000696422.1:c.869A=
ENST00000696423.1:c.872A=
ENST00000696424.1:c.858A=	ENSP00000512619.1:n.858A=
ENST00000696425.1:c.865-185A=	ENSP00000512620.1:n.865-185A=
ENST00000696426.1:c.*466A=	ENSP00000512621.1:n.*466A=
ENST00000696427.1:c.1013A=	ENSP00000512622.1:p.His338=
ENST00000696428.1:c.*848A=	ENSP00000512623.1:n.*848A=
ENST00000696429.1:c.1006A=	ENSP00000512624.1:p.Thr336=
ENST00000696430.1:c.1006A=	ENSP00000512625.1:p.Thr336=
ENST00000393562.10:c.1006A= MANE Select	ENSP00000377192.3:p.Thr336=
ENST00000369620.6:c.1144A=	ENSP00000358633.2:p.Thr382=
ENST00000393562.6:c.1096A=	ENSP00000377192.2:p.Thr366=
ENST00000393564.6:c.1006A=	ENSP00000377194.2:p.Thr336=
ENST00000439227.5:c.1009A=	ENSP00000395599.1:p.Thr337=
ENST00000490651.1:n.88A=
ENST00000621232.4:c.1006A=	ENSP00000483686.1:p.Thr336=
NM_000402.4:c.1096A=	NP_000393.4:p.Thr366=
NM_001042351.2:c.1006A=	NP_001035810.1:p.Thr336=
XM_005274657.2:c.1099A=	XP_005274714.1:p.Thr367=
XM_005274658.2:c.1009A=	XP_005274715.1:p.Thr337=
XM_011531132.1:c.958-185A=	XP_011529434.1:n.958-185A=
NM_001360016.2:c.1006A= MANE Select	NP_001346945.1:p.Thr336=
NM_001042351.3:c.1006A=	NP_001035810.1:p.Thr336=