Canonical Allele Identifier: CA415234843

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761311C>G (hg19) ; chrX:g.154533096C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533096C>G , CM000685.2:g.154533096C>G	GRCh38
NC_000023.10:g.153761311C>G , CM000685.1:g.153761311C>G	GRCh37
NC_000023.9:g.153414505C>G	NCBI36
NG_009015.2:g.19477G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.897G>C	ENSP00000377194.2:p.Gln299His
ENST00000439227.6:c.900G>C	ENSP00000395599.2:p.Gln300His
ENST00000696420.1:c.897G>C	ENSP00000512615.1:p.Gln299His
ENST00000696421.1:c.897G>C	ENSP00000512616.1:p.Gln299His
ENST00000696422.1:c.760G>C
ENST00000696423.1:c.763G>C
ENST00000696424.1:c.749G>C	ENSP00000512619.1:n.749G>C
ENST00000696425.1:c.865-294G>C	ENSP00000512620.1:n.865-294G>C
ENST00000696426.1:c.*357G>C	ENSP00000512621.1:n.*357G>C
ENST00000696427.1:c.904G>C	ENSP00000512622.1:p.Gly302Arg
ENST00000696428.1:c.*739G>C	ENSP00000512623.1:n.*739G>C
ENST00000696429.1:c.897G>C	ENSP00000512624.1:p.Gln299His
ENST00000696430.1:c.897G>C	ENSP00000512625.1:p.Gln299His
ENST00000393562.10:c.897G>C MANE Select	ENSP00000377192.3:p.Gln299His
ENST00000369620.6:c.1035G>C	ENSP00000358633.2:p.Gln345His
ENST00000393562.6:c.987G>C	ENSP00000377192.2:p.Gln329His
ENST00000393564.6:c.897G>C	ENSP00000377194.2:p.Gln299His
ENST00000439227.5:c.900G>C	ENSP00000395599.1:p.Gln300His
ENST00000440967.5:c.900G>C	ENSP00000400648.1:p.Gln300His
ENST00000621232.4:c.897G>C	ENSP00000483686.1:p.Gln299His
NM_000402.4:c.987G>C	NP_000393.4:p.Gln329His
NM_001042351.2:c.897G>C	NP_001035810.1:p.Gln299His
XM_005274657.2:c.990G>C	XP_005274714.1:p.Gln330His
XM_005274658.2:c.900G>C	XP_005274715.1:p.Gln300His
XM_011531132.1:c.958-294G>C	XP_011529434.1:n.958-294G>C
NM_001360016.2:c.897G>C MANE Select	NP_001346945.1:p.Gln299His
NM_001042351.3:c.897G>C	NP_001035810.1:p.Gln299His