Canonical Allele Identifier: CA519303624

Gene: G6PD

Linked Data

• dbSNP Id: rs2070360900
• MyVariant Identifiers: chrX:g.153761281C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533066C>A , CM000685.2:g.154533066C>A	GRCh38
NC_000023.10:g.153761281C>A , CM000685.1:g.153761281C>A	GRCh37
NC_000023.9:g.153414475C>A	NCBI36
NG_009015.2:g.19507G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.927G>T	ENSP00000377194.2:p.Val309=
ENST00000439227.6:c.930G>T	ENSP00000395599.2:p.Val310=
ENST00000696420.1:c.927G>T	ENSP00000512615.1:p.Val309=
ENST00000696421.1:c.927G>T	ENSP00000512616.1:p.Val309=
ENST00000696422.1:c.790G>T
ENST00000696423.1:c.793G>T
ENST00000696424.1:c.779G>T	ENSP00000512619.1:n.779G>T
ENST00000696425.1:c.865-264G>T	ENSP00000512620.1:n.865-264G>T
ENST00000696426.1:c.*387G>T	ENSP00000512621.1:n.*387G>T
ENST00000696427.1:c.934G>T	ENSP00000512622.1:p.Gly312Trp
ENST00000696428.1:c.*769G>T	ENSP00000512623.1:n.*769G>T
ENST00000696429.1:c.927G>T	ENSP00000512624.1:p.Val309=
ENST00000696430.1:c.927G>T	ENSP00000512625.1:p.Val309=
ENST00000393562.10:c.927G>T MANE Select	ENSP00000377192.3:p.Val309=
ENST00000369620.6:c.1065G>T	ENSP00000358633.2:p.Val355=
ENST00000393562.6:c.1017G>T	ENSP00000377192.2:p.Val339=
ENST00000393564.6:c.927G>T	ENSP00000377194.2:p.Val309=
ENST00000439227.5:c.930G>T	ENSP00000395599.1:p.Val310=
ENST00000440967.5:c.930G>T	ENSP00000400648.1:p.Val310=
ENST00000490651.1:n.9G>T
ENST00000621232.4:c.927G>T	ENSP00000483686.1:p.Val309=
NM_000402.4:c.1017G>T	NP_000393.4:p.Val339=
NM_001042351.2:c.927G>T	NP_001035810.1:p.Val309=
XM_005274657.2:c.1020G>T	XP_005274714.1:p.Val340=
XM_005274658.2:c.930G>T	XP_005274715.1:p.Val310=
XM_011531132.1:c.958-264G>T	XP_011529434.1:n.958-264G>T
NM_001360016.2:c.927G>T MANE Select	NP_001346945.1:p.Val309=
NM_001042351.3:c.927G>T	NP_001035810.1:p.Val309=