Canonical Allele Identifier: CA120994

Gene: G6PD

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532257C>T , CM000685.2:g.154532257C>T	GRCh38
NC_000023.10:g.153760472C>T , CM000685.1:g.153760472C>T	GRCh37
NC_000023.9:g.153413666C>T	NCBI36
NG_009015.2:g.20316G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1388G>A	ENSP00000377194.2:p.Arg463His
ENST00000439227.6:c.1391G>A	ENSP00000395599.2:p.Arg464His
ENST00000696420.1:c.1388G>A	ENSP00000512615.1:p.Arg463His
ENST00000696421.1:c.1388G>A	ENSP00000512616.1:p.Arg463His
ENST00000696422.1:c.1251G>A
ENST00000696423.1:c.1254G>A
ENST00000696424.1:c.1240G>A	ENSP00000512619.1:n.1240G>A
ENST00000696425.1:c.*301G>A	ENSP00000512620.1:n.*301G>A
ENST00000696426.1:c.*848G>A	ENSP00000512621.1:n.*848G>A
ENST00000696427.1:c.*348G>A	ENSP00000512622.1:n.*348G>A
ENST00000696428.1:c.*1230G>A	ENSP00000512623.1:n.*1230G>A
ENST00000696429.1:c.1388G>A	ENSP00000512624.1:p.Arg463His
ENST00000696430.1:c.1388G>A	ENSP00000512625.1:p.Arg463His
ENST00000393562.10:c.1388G>A MANE Select	ENSP00000377192.3:p.Arg463His
ENST00000369620.6:c.1526G>A	ENSP00000358633.2:p.Arg509His
ENST00000393562.6:c.1478G>A	ENSP00000377192.2:p.Arg493His
ENST00000393564.6:c.1388G>A	ENSP00000377194.2:p.Arg463His
ENST00000490651.1:n.609G>A
ENST00000621232.4:c.1388G>A	ENSP00000483686.1:p.Arg463His
NM_000402.4:c.1478G>A	NP_000393.4:p.Arg493His
NM_001042351.2:c.1388G>A	NP_001035810.1:p.Arg463His
XM_005274657.2:c.1481G>A	XP_005274714.1:p.Arg494His
XM_005274658.2:c.1391G>A	XP_005274715.1:p.Arg464His
NM_001360016.2:c.1388G>A MANE Select	NP_001346945.1:p.Arg463His
NM_001042351.3:c.1388G>A	NP_001035810.1:p.Arg463His