Canonical Allele Identifier: CA2824300338
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154532465_154532568del , CM000685.2:g.154532465_154532568del GRCh38
NC_000023.10:g.153760680_153760783del , CM000685.1:g.153760680_153760783del GRCh37
NC_000023.9:g.153413874_153413977del NCBI36
NG_009015.2:g.20007_20110del

Transcript Alleles

HGVS Amino-acid change
ENST00000393564.7:c.1287+1_1288-1del
ENST00000439227.6:c.1290+1_1291-1del
ENST00000696420.1:c.1287+1_1288-1del
ENST00000696421.1:c.1287+1_1288-1del
ENST00000696422.1:c.1150+1_1151-1del
ENST00000696423.1:c.1153+1_1154-1del
ENST00000696424.1:c.1139+1_1140-1del
ENST00000696425.1:c.*200+1_*201-1del
ENST00000696426.1:c.*747+1_*748-1del
ENST00000696427.1:c.*247+1_*248-1del
ENST00000696428.1:c.*1129+1_*1130-1del
ENST00000696429.1:c.1287+1_1288-1del
ENST00000696430.1:c.1287+1_1288-1del
ENST00000393562.10:c.1287+1_1288-1del
ENST00000369620.6:c.1425+1_1426-1del
ENST00000393562.6:c.1377+1_1378-1del
ENST00000393564.6:c.1287+1_1288-1del
ENST00000490651.1:n.508+1_509-1del
ENST00000621232.4:c.1287+1_1288-1del
NM_000402.4:c.1377+1_1378-1del
NM_001042351.2:c.1287+1_1288-1del
XM_005274657.2:c.1380+1_1381-1del
XM_005274658.2:c.1290+1_1291-1del
NM_001360016.2:c.1287+1_1288-1del
NM_001042351.3:c.1287+1_1288-1del