Canonical Allele Identifier: CA645291633
Gene: G6PD HGNC NCBI

Linked Data

dbSNP Id: rs1569556185
MyVariant Identifiers: chrX:g.153760379del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154532167del , CM000685.2:g.154532167del GRCh38
NC_000023.10:g.153760382del , CM000685.1:g.153760382del GRCh37
NC_000023.9:g.153413576del NCBI36
NG_009015.2:g.20409del

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.1457+24del ENSP00000377194.2:n.1457+24del
ENST00000439227.6:c.1460+24del ENSP00000395599.2:n.1460+24del
ENST00000696420.1:c.1457+24del ENSP00000512615.1:n.1457+24del
ENST00000696421.1:c.1457+24del ENSP00000512616.1:n.1457+24del
ENST00000696422.1:c.1320+24del
ENST00000696423.1:c.1323+24del
ENST00000696424.1:c.1309+24del ENSP00000512619.1:n.1309+24del
ENST00000696425.1:c.*370+24del ENSP00000512620.1:n.*370+24del
ENST00000696426.1:c.*917+24del ENSP00000512621.1:n.*917+24del
ENST00000696427.1:c.*417+24del ENSP00000512622.1:n.*417+24del
ENST00000696428.1:c.*1299+24del ENSP00000512623.1:n.*1299+24del
ENST00000696429.1:c.1457+24del ENSP00000512624.1:n.1457+24del
ENST00000696430.1:c.1457+24del ENSP00000512625.1:n.1457+24del
ENST00000393562.10:c.1457+24del MANE Select ENSP00000377192.3:n.1457+24del
ENST00000369620.6:c.1595+24del ENSP00000358633.2:n.1595+24del
ENST00000393562.6:c.1547+24del ENSP00000377192.2:n.1547+24del
ENST00000393564.6:c.1457+24del ENSP00000377194.2:n.1457+24del
ENST00000490651.1:n.702del
ENST00000621232.4:c.1457+24del ENSP00000483686.1:n.1457+24del
NM_000402.4:c.1547+24del NP_000393.4:n.1547+24del
NM_001042351.2:c.1457+24del NP_001035810.1:n.1457+24del
XM_005274657.2:c.1550+24del XP_005274714.1:n.1550+24del
XM_005274658.2:c.1460+24del XP_005274715.1:n.1460+24del
NM_001360016.2:c.1457+24del MANE Select NP_001346945.1:n.1457+24del
NM_001042351.3:c.1457+24del NP_001035810.1:n.1457+24del