Canonical Allele Identifier: CA415234002

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760868A>C (hg19) ; chrX:g.154532653A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532653A>C , CM000685.2:g.154532653A>C	GRCh38
NC_000023.10:g.153760868A>C , CM000685.1:g.153760868A>C	GRCh37
NC_000023.9:g.153414062A>C	NCBI36
NG_009015.2:g.19920T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1201T>G	ENSP00000377194.2:p.Tyr401Asp
ENST00000439227.6:c.1204T>G	ENSP00000395599.2:p.Tyr402Asp
ENST00000696420.1:c.1201T>G	ENSP00000512615.1:p.Tyr401Asp
ENST00000696421.1:c.1201T>G	ENSP00000512616.1:p.Tyr401Asp
ENST00000696422.1:c.1064T>G
ENST00000696423.1:c.1067T>G
ENST00000696424.1:c.1053T>G	ENSP00000512619.1:n.1053T>G
ENST00000696425.1:c.*114T>G	ENSP00000512620.1:n.*114T>G
ENST00000696426.1:c.*661T>G	ENSP00000512621.1:n.*661T>G
ENST00000696427.1:c.*161T>G	ENSP00000512622.1:n.*161T>G
ENST00000696428.1:c.*1043T>G	ENSP00000512623.1:n.*1043T>G
ENST00000696429.1:c.1201T>G	ENSP00000512624.1:p.Tyr401Asp
ENST00000696430.1:c.1201T>G	ENSP00000512625.1:p.Tyr401Asp
ENST00000393562.10:c.1201T>G MANE Select	ENSP00000377192.3:p.Tyr401Asp
ENST00000369620.6:c.1339T>G	ENSP00000358633.2:p.Tyr447Asp
ENST00000393562.6:c.1291T>G	ENSP00000377192.2:p.Tyr431Asp
ENST00000393564.6:c.1201T>G	ENSP00000377194.2:p.Tyr401Asp
ENST00000490651.1:n.422T>G
ENST00000621232.4:c.1201T>G	ENSP00000483686.1:p.Tyr401Asp
NM_000402.4:c.1291T>G	NP_000393.4:p.Tyr431Asp
NM_001042351.2:c.1201T>G	NP_001035810.1:p.Tyr401Asp
XM_005274657.2:c.1294T>G	XP_005274714.1:p.Tyr432Asp
XM_005274658.2:c.1204T>G	XP_005274715.1:p.Tyr402Asp
XM_011531132.1:c.*114T>G	XP_011529434.1:n.*114T>G
NM_001360016.2:c.1201T>G MANE Select	NP_001346945.1:p.Tyr401Asp
NM_001042351.3:c.1201T>G	NP_001035810.1:p.Tyr401Asp