Canonical Allele Identifier: CA120950
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154532439A= , CM000685.2:g.154532439A= GRCh38
NG_009015.2:g.20134T=

Transcript Alleles

HGVS Amino-acid Change
NM_001360016.2:c.1311T= MANE Select NP_001346945.1:p.Tyr437=
ENST00000393562.10:c.1311T= MANE Select ENSP00000377192.3:p.Tyr437=
NM_000402.4:c.1401T= NP_000393.4:p.Tyr467=
NM_001042351.2:c.1311T= NP_001035810.1:p.Tyr437=
NM_001042351.3:c.1311T= NP_001035810.1:p.Tyr437=
ENST00000369620.6:c.1449T= ENSP00000358633.2:p.Tyr483=
ENST00000393562.6:c.1401T= ENSP00000377192.2:p.Tyr467=
ENST00000393564.6:c.1311T= ENSP00000377194.2:p.Tyr437=
ENST00000393564.7:c.1311T= ENSP00000377194.2:p.Tyr437=
ENST00000439227.6:c.1314T= ENSP00000395599.2:p.Tyr438=
ENST00000490651.1:n.532T=
ENST00000621232.4:c.1311T= ENSP00000483686.1:p.Tyr437=
ENST00000696420.1:c.1311T= ENSP00000512615.1:p.Tyr437=
ENST00000696421.1:c.1311T= ENSP00000512616.1:p.Tyr437=
ENST00000696422.1:c.1174T=
ENST00000696423.1:c.1177T=
ENST00000696424.1:c.1163T= ENSP00000512619.1:n.1163T=
ENST00000696425.1:c.*224T= ENSP00000512620.1:n.*224T=
ENST00000696426.1:c.*771T= ENSP00000512621.1:n.*771T=
ENST00000696427.1:c.*271T= ENSP00000512622.1:n.*271T=
ENST00000696428.1:c.*1153T= ENSP00000512623.1:n.*1153T=
ENST00000696429.1:c.1311T= ENSP00000512624.1:p.Tyr437=
ENST00000696430.1:c.1311T= ENSP00000512625.1:p.Tyr437=
XM_005274657.2:c.1404T= XP_005274714.1:p.Tyr468=
XM_005274658.2:c.1314T= XP_005274715.1:p.Tyr438=