Canonical Allele Identifier: CA415231946

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760259G>C (hg19) ; chrX:g.154532044G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532044G>C , CM000685.2:g.154532044G>C	GRCh38
NC_000023.10:g.153760259G>C , CM000685.1:g.153760259G>C	GRCh37
NC_000023.9:g.153413453G>C	NCBI36
NG_009015.2:g.20529C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1504C>G	ENSP00000377194.2:p.Gln502Glu
ENST00000439227.6:c.1507C>G	ENSP00000395599.2:p.Gln503Glu
ENST00000696420.1:c.1457+144C>G	ENSP00000512615.1:n.1457+144C>G
ENST00000696421.1:c.1457+144C>G	ENSP00000512616.1:n.1457+144C>G
ENST00000696422.1:c.1367C>G
ENST00000696423.1:c.1370C>G
ENST00000696424.1:c.1356C>G	ENSP00000512619.1:n.1356C>G
ENST00000696425.1:c.*417C>G	ENSP00000512620.1:n.*417C>G
ENST00000696426.1:c.*964C>G	ENSP00000512621.1:n.*964C>G
ENST00000696427.1:c.*464C>G	ENSP00000512622.1:n.*464C>G
ENST00000696428.1:c.*1346C>G	ENSP00000512623.1:n.*1346C>G
ENST00000696429.1:c.1504C>G	ENSP00000512624.1:p.Gln502Glu
ENST00000696430.1:c.1504C>G	ENSP00000512625.1:p.Gln502Glu
ENST00000393562.10:c.1504C>G MANE Select	ENSP00000377192.3:p.Gln502Glu
ENST00000369620.6:c.1642C>G	ENSP00000358633.2:p.Gln548Glu
ENST00000393562.6:c.1594C>G	ENSP00000377192.2:p.Gln532Glu
ENST00000393564.6:c.1504C>G	ENSP00000377194.2:p.Gln502Glu
ENST00000621232.4:c.1504C>G	ENSP00000483686.1:p.Gln502Glu
NM_000402.4:c.1594C>G	NP_000393.4:p.Gln532Glu
NM_001042351.2:c.1504C>G	NP_001035810.1:p.Gln502Glu
XM_005274657.2:c.1597C>G	XP_005274714.1:p.Gln533Glu
XM_005274658.2:c.1507C>G	XP_005274715.1:p.Gln503Glu
NM_001360016.2:c.1504C>G MANE Select	NP_001346945.1:p.Gln502Glu
NM_001042351.3:c.1504C>G	NP_001035810.1:p.Gln502Glu