Canonical Allele Identifier: CA337316624
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 3032932
ClinVar RCV Id: RCV003894570
dbSNP Id: rs782593777

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154533012C>T , CM000685.2:g.154533012C>T GRCh38
NC_000023.10:g.153761227C>T , CM000685.1:g.153761227C>T GRCh37
NC_000023.9:g.153414421C>T NCBI36
NG_009015.2:g.19561G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.981G>A ENSP00000377194.2:p.Thr327=
ENST00000439227.6:c.984G>A ENSP00000395599.2:p.Thr328=
ENST00000696420.1:c.981G>A ENSP00000512615.1:p.Thr327=
ENST00000696421.1:c.981G>A ENSP00000512616.1:p.Thr327=
ENST00000696422.1:c.844G>A
ENST00000696423.1:c.847G>A
ENST00000696424.1:c.833G>A ENSP00000512619.1:n.833G>A
ENST00000696425.1:c.865-210G>A ENSP00000512620.1:n.865-210G>A
ENST00000696426.1:c.*441G>A ENSP00000512621.1:n.*441G>A
ENST00000696427.1:c.988G>A ENSP00000512622.1:p.Gly330Ser
ENST00000696428.1:c.*823G>A ENSP00000512623.1:n.*823G>A
ENST00000696429.1:c.981G>A ENSP00000512624.1:p.Thr327=
ENST00000696430.1:c.981G>A ENSP00000512625.1:p.Thr327=
ENST00000393562.10:c.981G>A MANE Select ENSP00000377192.3:p.Thr327=
ENST00000369620.6:c.1119G>A ENSP00000358633.2:p.Thr373=
ENST00000393562.6:c.1071G>A ENSP00000377192.2:p.Thr357=
ENST00000393564.6:c.981G>A ENSP00000377194.2:p.Thr327=
ENST00000439227.5:c.984G>A ENSP00000395599.1:p.Thr328=
ENST00000490651.1:n.63G>A
ENST00000621232.4:c.981G>A ENSP00000483686.1:p.Thr327=
NM_000402.4:c.1071G>A NP_000393.4:p.Thr357=
NM_001042351.2:c.981G>A NP_001035810.1:p.Thr327=
XM_005274657.2:c.1074G>A XP_005274714.1:p.Thr358=
XM_005274658.2:c.984G>A XP_005274715.1:p.Thr328=
XM_011531132.1:c.958-210G>A XP_011529434.1:n.958-210G>A
NM_001360016.2:c.981G>A MANE Select NP_001346945.1:p.Thr327=
NM_001042351.3:c.981G>A NP_001035810.1:p.Thr327=