Canonical Allele Identifier: CA415234491

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761229T>A (hg19) ; chrX:g.154533014T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533014T>A , CM000685.2:g.154533014T>A	GRCh38
NC_000023.10:g.153761229T>A , CM000685.1:g.153761229T>A	GRCh37
NC_000023.9:g.153414423T>A	NCBI36
NG_009015.2:g.19559A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.979A>T	ENSP00000377194.2:p.Thr327Ser
ENST00000439227.6:c.982A>T	ENSP00000395599.2:p.Thr328Ser
ENST00000696420.1:c.979A>T	ENSP00000512615.1:p.Thr327Ser
ENST00000696421.1:c.979A>T	ENSP00000512616.1:p.Thr327Ser
ENST00000696422.1:c.842A>T
ENST00000696423.1:c.845A>T
ENST00000696424.1:c.831A>T	ENSP00000512619.1:n.831A>T
ENST00000696425.1:c.865-212A>T	ENSP00000512620.1:n.865-212A>T
ENST00000696426.1:c.*439A>T	ENSP00000512621.1:n.*439A>T
ENST00000696427.1:c.986A>T	ENSP00000512622.1:p.His329Leu
ENST00000696428.1:c.*821A>T	ENSP00000512623.1:n.*821A>T
ENST00000696429.1:c.979A>T	ENSP00000512624.1:p.Thr327Ser
ENST00000696430.1:c.979A>T	ENSP00000512625.1:p.Thr327Ser
ENST00000393562.10:c.979A>T MANE Select	ENSP00000377192.3:p.Thr327Ser
ENST00000369620.6:c.1117A>T	ENSP00000358633.2:p.Thr373Ser
ENST00000393562.6:c.1069A>T	ENSP00000377192.2:p.Thr357Ser
ENST00000393564.6:c.979A>T	ENSP00000377194.2:p.Thr327Ser
ENST00000439227.5:c.982A>T	ENSP00000395599.1:p.Thr328Ser
ENST00000490651.1:n.61A>T
ENST00000621232.4:c.979A>T	ENSP00000483686.1:p.Thr327Ser
NM_000402.4:c.1069A>T	NP_000393.4:p.Thr357Ser
NM_001042351.2:c.979A>T	NP_001035810.1:p.Thr327Ser
XM_005274657.2:c.1072A>T	XP_005274714.1:p.Thr358Ser
XM_005274658.2:c.982A>T	XP_005274715.1:p.Thr328Ser
XM_011531132.1:c.958-212A>T	XP_011529434.1:n.958-212A>T
NM_001360016.2:c.979A>T MANE Select	NP_001346945.1:p.Thr327Ser
NM_001042351.3:c.979A>T	NP_001035810.1:p.Thr327Ser