Canonical Allele Identifier: CA519303230

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761164C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532949C>T , CM000685.2:g.154532949C>T	GRCh38
NC_000023.10:g.153761164C>T , CM000685.1:g.153761164C>T	GRCh37
NC_000023.9:g.153414358C>T	NCBI36
NG_009015.2:g.19624G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1044G>A	ENSP00000377194.2:p.Arg348=
ENST00000439227.6:c.1047G>A	ENSP00000395599.2:p.Arg349=
ENST00000696420.1:c.1044G>A	ENSP00000512615.1:p.Arg348=
ENST00000696421.1:c.1044G>A	ENSP00000512616.1:p.Arg348=
ENST00000696422.1:c.907G>A
ENST00000696423.1:c.910G>A
ENST00000696424.1:c.896G>A	ENSP00000512619.1:n.896G>A
ENST00000696425.1:c.865-147G>A	ENSP00000512620.1:n.865-147G>A
ENST00000696426.1:c.*504G>A	ENSP00000512621.1:n.*504G>A
ENST00000696427.1:c.*4G>A	ENSP00000512622.1:n.*4G>A
ENST00000696428.1:c.*886G>A	ENSP00000512623.1:n.*886G>A
ENST00000696429.1:c.1044G>A	ENSP00000512624.1:p.Arg348=
ENST00000696430.1:c.1044G>A	ENSP00000512625.1:p.Arg348=
ENST00000393562.10:c.1044G>A MANE Select	ENSP00000377192.3:p.Arg348=
ENST00000369620.6:c.1182G>A	ENSP00000358633.2:p.Arg394=
ENST00000393562.6:c.1134G>A	ENSP00000377192.2:p.Arg378=
ENST00000393564.6:c.1044G>A	ENSP00000377194.2:p.Arg348=
ENST00000490651.1:n.126G>A
ENST00000621232.4:c.1044G>A	ENSP00000483686.1:p.Arg348=
NM_000402.4:c.1134G>A	NP_000393.4:p.Arg378=
NM_001042351.2:c.1044G>A	NP_001035810.1:p.Arg348=
XM_005274657.2:c.1137G>A	XP_005274714.1:p.Arg379=
XM_005274658.2:c.1047G>A	XP_005274715.1:p.Arg349=
XM_011531132.1:c.958-147G>A	XP_011529434.1:n.958-147G>A
NM_001360016.2:c.1044G>A MANE Select	NP_001346945.1:p.Arg348=
NM_001042351.3:c.1044G>A	NP_001035810.1:p.Arg348=