Canonical Allele Identifier: CA415233912

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760831A>T (hg19) ; chrX:g.154532616A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532616A>T , CM000685.2:g.154532616A>T	GRCh38
NC_000023.10:g.153760831A>T , CM000685.1:g.153760831A>T	GRCh37
NC_000023.9:g.153414025A>T	NCBI36
NG_009015.2:g.19957T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1238T>A	ENSP00000377194.2:p.Phe413Tyr
ENST00000439227.6:c.1241T>A	ENSP00000395599.2:p.Phe414Tyr
ENST00000696420.1:c.1238T>A	ENSP00000512615.1:p.Phe413Tyr
ENST00000696421.1:c.1238T>A	ENSP00000512616.1:p.Phe413Tyr
ENST00000696422.1:c.1101T>A
ENST00000696423.1:c.1104T>A
ENST00000696424.1:c.1090T>A	ENSP00000512619.1:n.1090T>A
ENST00000696425.1:c.*151T>A	ENSP00000512620.1:n.*151T>A
ENST00000696426.1:c.*698T>A	ENSP00000512621.1:n.*698T>A
ENST00000696427.1:c.*198T>A	ENSP00000512622.1:n.*198T>A
ENST00000696428.1:c.*1080T>A	ENSP00000512623.1:n.*1080T>A
ENST00000696429.1:c.1238T>A	ENSP00000512624.1:p.Phe413Tyr
ENST00000696430.1:c.1238T>A	ENSP00000512625.1:p.Phe413Tyr
ENST00000393562.10:c.1238T>A MANE Select	ENSP00000377192.3:p.Phe413Tyr
ENST00000369620.6:c.1376T>A	ENSP00000358633.2:p.Phe459Tyr
ENST00000393562.6:c.1328T>A	ENSP00000377192.2:p.Phe443Tyr
ENST00000393564.6:c.1238T>A	ENSP00000377194.2:p.Phe413Tyr
ENST00000490651.1:n.459T>A
ENST00000621232.4:c.1238T>A	ENSP00000483686.1:p.Phe413Tyr
NM_000402.4:c.1328T>A	NP_000393.4:p.Phe443Tyr
NM_001042351.2:c.1238T>A	NP_001035810.1:p.Phe413Tyr
XM_005274657.2:c.1331T>A	XP_005274714.1:p.Phe444Tyr
XM_005274658.2:c.1241T>A	XP_005274715.1:p.Phe414Tyr
XM_011531132.1:c.*151T>A	XP_011529434.1:n.*151T>A
NM_001360016.2:c.1238T>A MANE Select	NP_001346945.1:p.Phe413Tyr
NM_001042351.3:c.1238T>A	NP_001035810.1:p.Phe413Tyr