Canonical Allele Identifier: CA415234600

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761255G>C (hg19) ; chrX:g.154533040G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533040G>C , CM000685.2:g.154533040G>C	GRCh38
NC_000023.10:g.153761255G>C , CM000685.1:g.153761255G>C	GRCh37
NC_000023.9:g.153414449G>C	NCBI36
NG_009015.2:g.19533C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.953C>G	ENSP00000377194.2:p.Ala318Gly
ENST00000439227.6:c.956C>G	ENSP00000395599.2:p.Ala319Gly
ENST00000696420.1:c.953C>G	ENSP00000512615.1:p.Ala318Gly
ENST00000696421.1:c.953C>G	ENSP00000512616.1:p.Ala318Gly
ENST00000696422.1:c.816C>G
ENST00000696423.1:c.819C>G
ENST00000696424.1:c.805C>G	ENSP00000512619.1:n.805C>G
ENST00000696425.1:c.865-238C>G	ENSP00000512620.1:n.865-238C>G
ENST00000696426.1:c.*413C>G	ENSP00000512621.1:n.*413C>G
ENST00000696427.1:c.960C>G	ENSP00000512622.1:p.Gly320=
ENST00000696428.1:c.*795C>G	ENSP00000512623.1:n.*795C>G
ENST00000696429.1:c.953C>G	ENSP00000512624.1:p.Ala318Gly
ENST00000696430.1:c.953C>G	ENSP00000512625.1:p.Ala318Gly
ENST00000393562.10:c.953C>G MANE Select	ENSP00000377192.3:p.Ala318Gly
ENST00000369620.6:c.1091C>G	ENSP00000358633.2:p.Ala364Gly
ENST00000393562.6:c.1043C>G	ENSP00000377192.2:p.Ala348Gly
ENST00000393564.6:c.953C>G	ENSP00000377194.2:p.Ala318Gly
ENST00000439227.5:c.956C>G	ENSP00000395599.1:p.Ala319Gly
ENST00000440967.5:c.956C>G	ENSP00000400648.1:p.Ala319Gly
ENST00000490651.1:n.35C>G
ENST00000621232.4:c.953C>G	ENSP00000483686.1:p.Ala318Gly
NM_000402.4:c.1043C>G	NP_000393.4:p.Ala348Gly
NM_001042351.2:c.953C>G	NP_001035810.1:p.Ala318Gly
XM_005274657.2:c.1046C>G	XP_005274714.1:p.Ala349Gly
XM_005274658.2:c.956C>G	XP_005274715.1:p.Ala319Gly
XM_011531132.1:c.958-238C>G	XP_011529434.1:n.958-238C>G
NM_001360016.2:c.953C>G MANE Select	NP_001346945.1:p.Ala318Gly
NM_001042351.3:c.953C>G	NP_001035810.1:p.Ala318Gly