Canonical Allele Identifier: CA415234609

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761256C>T (hg19) ; chrX:g.154533041C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533041C>T , CM000685.2:g.154533041C>T	GRCh38
NC_000023.10:g.153761256C>T , CM000685.1:g.153761256C>T	GRCh37
NC_000023.9:g.153414450C>T	NCBI36
NG_009015.2:g.19532G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.952G>A	ENSP00000377194.2:p.Ala318Thr
ENST00000439227.6:c.955G>A	ENSP00000395599.2:p.Ala319Thr
ENST00000696420.1:c.952G>A	ENSP00000512615.1:p.Ala318Thr
ENST00000696421.1:c.952G>A	ENSP00000512616.1:p.Ala318Thr
ENST00000696422.1:c.815G>A
ENST00000696423.1:c.818G>A
ENST00000696424.1:c.804G>A	ENSP00000512619.1:n.804G>A
ENST00000696425.1:c.865-239G>A	ENSP00000512620.1:n.865-239G>A
ENST00000696426.1:c.*412G>A	ENSP00000512621.1:n.*412G>A
ENST00000696427.1:c.959G>A	ENSP00000512622.1:p.Gly320Asp
ENST00000696428.1:c.*794G>A	ENSP00000512623.1:n.*794G>A
ENST00000696429.1:c.952G>A	ENSP00000512624.1:p.Ala318Thr
ENST00000696430.1:c.952G>A	ENSP00000512625.1:p.Ala318Thr
ENST00000393562.10:c.952G>A MANE Select	ENSP00000377192.3:p.Ala318Thr
ENST00000369620.6:c.1090G>A	ENSP00000358633.2:p.Ala364Thr
ENST00000393562.6:c.1042G>A	ENSP00000377192.2:p.Ala348Thr
ENST00000393564.6:c.952G>A	ENSP00000377194.2:p.Ala318Thr
ENST00000439227.5:c.955G>A	ENSP00000395599.1:p.Ala319Thr
ENST00000440967.5:c.955G>A	ENSP00000400648.1:p.Ala319Thr
ENST00000490651.1:n.34G>A
ENST00000621232.4:c.952G>A	ENSP00000483686.1:p.Ala318Thr
NM_000402.4:c.1042G>A	NP_000393.4:p.Ala348Thr
NM_001042351.2:c.952G>A	NP_001035810.1:p.Ala318Thr
XM_005274657.2:c.1045G>A	XP_005274714.1:p.Ala349Thr
XM_005274658.2:c.955G>A	XP_005274715.1:p.Ala319Thr
XM_011531132.1:c.958-239G>A	XP_011529434.1:n.958-239G>A
NM_001360016.2:c.952G>A MANE Select	NP_001346945.1:p.Ala318Thr
NM_001042351.3:c.952G>A	NP_001035810.1:p.Ala318Thr