Canonical Allele Identifier: CA415234808

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761303T>A (hg19) ; chrX:g.154533088T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533088T>A , CM000685.2:g.154533088T>A	GRCh38
NC_000023.10:g.153761303T>A , CM000685.1:g.153761303T>A	GRCh37
NC_000023.9:g.153414497T>A	NCBI36
NG_009015.2:g.19485A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.905A>T	ENSP00000377194.2:p.Asn302Ile
ENST00000439227.6:c.908A>T	ENSP00000395599.2:p.Asn303Ile
ENST00000696420.1:c.905A>T	ENSP00000512615.1:p.Asn302Ile
ENST00000696421.1:c.905A>T	ENSP00000512616.1:p.Asn302Ile
ENST00000696422.1:c.768A>T
ENST00000696423.1:c.771A>T
ENST00000696424.1:c.757A>T	ENSP00000512619.1:n.757A>T
ENST00000696425.1:c.865-286A>T	ENSP00000512620.1:n.865-286A>T
ENST00000696426.1:c.*365A>T	ENSP00000512621.1:n.*365A>T
ENST00000696427.1:c.912A>T	ENSP00000512622.1:p.Gln304His
ENST00000696428.1:c.*747A>T	ENSP00000512623.1:n.*747A>T
ENST00000696429.1:c.905A>T	ENSP00000512624.1:p.Asn302Ile
ENST00000696430.1:c.905A>T	ENSP00000512625.1:p.Asn302Ile
ENST00000393562.10:c.905A>T MANE Select	ENSP00000377192.3:p.Asn302Ile
ENST00000369620.6:c.1043A>T	ENSP00000358633.2:p.Asn348Ile
ENST00000393562.6:c.995A>T	ENSP00000377192.2:p.Asn332Ile
ENST00000393564.6:c.905A>T	ENSP00000377194.2:p.Asn302Ile
ENST00000439227.5:c.908A>T	ENSP00000395599.1:p.Asn303Ile
ENST00000440967.5:c.908A>T	ENSP00000400648.1:p.Asn303Ile
ENST00000621232.4:c.905A>T	ENSP00000483686.1:p.Asn302Ile
NM_000402.4:c.995A>T	NP_000393.4:p.Asn332Ile
NM_001042351.2:c.905A>T	NP_001035810.1:p.Asn302Ile
XM_005274657.2:c.998A>T	XP_005274714.1:p.Asn333Ile
XM_005274658.2:c.908A>T	XP_005274715.1:p.Asn303Ile
XM_011531132.1:c.958-286A>T	XP_011529434.1:n.958-286A>T
NM_001360016.2:c.905A>T MANE Select	NP_001346945.1:p.Asn302Ile
NM_001042351.3:c.905A>T	NP_001035810.1:p.Asn302Ile