Canonical Allele Identifier: CA519302781

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760245G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532030G>C , CM000685.2:g.154532030G>C	GRCh38
NC_000023.10:g.153760245G>C , CM000685.1:g.153760245G>C	GRCh37
NC_000023.9:g.153413439G>C	NCBI36
NG_009015.2:g.20543C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1518C>G	ENSP00000377194.2:p.Thr506=
ENST00000439227.6:c.1521C>G	ENSP00000395599.2:p.Thr507=
ENST00000696420.1:c.1457+158C>G	ENSP00000512615.1:n.1457+158C>G
ENST00000696421.1:c.1457+158C>G	ENSP00000512616.1:n.1457+158C>G
ENST00000696422.1:c.1381C>G
ENST00000696423.1:c.1384C>G
ENST00000696424.1:c.1370C>G	ENSP00000512619.1:n.1370C>G
ENST00000696425.1:c.*431C>G	ENSP00000512620.1:n.*431C>G
ENST00000696426.1:c.*978C>G	ENSP00000512621.1:n.*978C>G
ENST00000696427.1:c.*478C>G	ENSP00000512622.1:n.*478C>G
ENST00000696428.1:c.*1360C>G	ENSP00000512623.1:n.*1360C>G
ENST00000696429.1:c.1518C>G	ENSP00000512624.1:p.Thr506=
ENST00000696430.1:c.1518C>G	ENSP00000512625.1:p.Thr506=
ENST00000393562.10:c.1518C>G MANE Select	ENSP00000377192.3:p.Thr506=
ENST00000369620.6:c.1656C>G	ENSP00000358633.2:p.Thr552=
ENST00000393562.6:c.1608C>G	ENSP00000377192.2:p.Thr536=
ENST00000393564.6:c.1518C>G	ENSP00000377194.2:p.Thr506=
ENST00000621232.4:c.1518C>G	ENSP00000483686.1:p.Thr506=
NM_000402.4:c.1608C>G	NP_000393.4:p.Thr536=
NM_001042351.2:c.1518C>G	NP_001035810.1:p.Thr506=
XM_005274657.2:c.1611C>G	XP_005274714.1:p.Thr537=
XM_005274658.2:c.1521C>G	XP_005274715.1:p.Thr507=
NM_001360016.2:c.1518C>G MANE Select	NP_001346945.1:p.Thr506=
NM_001042351.3:c.1518C>G	NP_001035810.1:p.Thr506=