Canonical Allele Identifier: CA415232439

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760437C>T (hg19) ; chrX:g.154532222C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532222C>T , CM000685.2:g.154532222C>T	GRCh38
NC_000023.10:g.153760437C>T , CM000685.1:g.153760437C>T	GRCh37
NC_000023.9:g.153413631C>T	NCBI36
NG_009015.2:g.20351G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1423G>A	ENSP00000377194.2:p.Glu475Lys
ENST00000439227.6:c.1426G>A	ENSP00000395599.2:p.Glu476Lys
ENST00000696420.1:c.1423G>A	ENSP00000512615.1:p.Glu475Lys
ENST00000696421.1:c.1423G>A	ENSP00000512616.1:p.Glu475Lys
ENST00000696422.1:c.1286G>A
ENST00000696423.1:c.1289G>A
ENST00000696424.1:c.1275G>A	ENSP00000512619.1:n.1275G>A
ENST00000696425.1:c.*336G>A	ENSP00000512620.1:n.*336G>A
ENST00000696426.1:c.*883G>A	ENSP00000512621.1:n.*883G>A
ENST00000696427.1:c.*383G>A	ENSP00000512622.1:n.*383G>A
ENST00000696428.1:c.*1265G>A	ENSP00000512623.1:n.*1265G>A
ENST00000696429.1:c.1423G>A	ENSP00000512624.1:p.Glu475Lys
ENST00000696430.1:c.1423G>A	ENSP00000512625.1:p.Glu475Lys
ENST00000393562.10:c.1423G>A MANE Select	ENSP00000377192.3:p.Glu475Lys
ENST00000369620.6:c.1561G>A	ENSP00000358633.2:p.Glu521Lys
ENST00000393562.6:c.1513G>A	ENSP00000377192.2:p.Glu505Lys
ENST00000393564.6:c.1423G>A	ENSP00000377194.2:p.Glu475Lys
ENST00000490651.1:n.644G>A
ENST00000621232.4:c.1423G>A	ENSP00000483686.1:p.Glu475Lys
NM_000402.4:c.1513G>A	NP_000393.4:p.Glu505Lys
NM_001042351.2:c.1423G>A	NP_001035810.1:p.Glu475Lys
XM_005274657.2:c.1516G>A	XP_005274714.1:p.Glu506Lys
XM_005274658.2:c.1426G>A	XP_005274715.1:p.Glu476Lys
NM_001360016.2:c.1423G>A MANE Select	NP_001346945.1:p.Glu475Lys
NM_001042351.3:c.1423G>A	NP_001035810.1:p.Glu475Lys