Canonical Allele Identifier: CA415231882

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760247T>C (hg19) ; chrX:g.154532032T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532032T>C , CM000685.2:g.154532032T>C	GRCh38
NC_000023.10:g.153760247T>C , CM000685.1:g.153760247T>C	GRCh37
NC_000023.9:g.153413441T>C	NCBI36
NG_009015.2:g.20541A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1516A>G	ENSP00000377194.2:p.Thr506Ala
ENST00000439227.6:c.1519A>G	ENSP00000395599.2:p.Thr507Ala
ENST00000696420.1:c.1457+156A>G	ENSP00000512615.1:n.1457+156A>G
ENST00000696421.1:c.1457+156A>G	ENSP00000512616.1:n.1457+156A>G
ENST00000696422.1:c.1379A>G
ENST00000696423.1:c.1382A>G
ENST00000696424.1:c.1368A>G	ENSP00000512619.1:n.1368A>G
ENST00000696425.1:c.*429A>G	ENSP00000512620.1:n.*429A>G
ENST00000696426.1:c.*976A>G	ENSP00000512621.1:n.*976A>G
ENST00000696427.1:c.*476A>G	ENSP00000512622.1:n.*476A>G
ENST00000696428.1:c.*1358A>G	ENSP00000512623.1:n.*1358A>G
ENST00000696429.1:c.1516A>G	ENSP00000512624.1:p.Thr506Ala
ENST00000696430.1:c.1516A>G	ENSP00000512625.1:p.Thr506Ala
ENST00000393562.10:c.1516A>G MANE Select	ENSP00000377192.3:p.Thr506Ala
ENST00000369620.6:c.1654A>G	ENSP00000358633.2:p.Thr552Ala
ENST00000393562.6:c.1606A>G	ENSP00000377192.2:p.Thr536Ala
ENST00000393564.6:c.1516A>G	ENSP00000377194.2:p.Thr506Ala
ENST00000621232.4:c.1516A>G	ENSP00000483686.1:p.Thr506Ala
NM_000402.4:c.1606A>G	NP_000393.4:p.Thr536Ala
NM_001042351.2:c.1516A>G	NP_001035810.1:p.Thr506Ala
XM_005274657.2:c.1609A>G	XP_005274714.1:p.Thr537Ala
XM_005274658.2:c.1519A>G	XP_005274715.1:p.Thr507Ala
NM_001360016.2:c.1516A>G MANE Select	NP_001346945.1:p.Thr506Ala
NM_001042351.3:c.1516A>G	NP_001035810.1:p.Thr506Ala