Canonical Allele Identifier: CA2466723212
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154532158C= , CM000685.2:g.154532158C= GRCh38
NC_000023.10:g.153760373C= , CM000685.1:g.153760373C= GRCh37
NC_000023.9:g.153413567C= NCBI36
NG_009015.2:g.20415G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.1457+30G= ENSP00000377194.2:n.1457+30G=
ENST00000439227.6:c.1460+30G= ENSP00000395599.2:n.1460+30G=
ENST00000696420.1:c.1457+30G= ENSP00000512615.1:n.1457+30G=
ENST00000696421.1:c.1457+30G= ENSP00000512616.1:n.1457+30G=
ENST00000696422.1:c.1320+30G=
ENST00000696423.1:c.1323+30G=
ENST00000696424.1:c.1309+30G= ENSP00000512619.1:n.1309+30G=
ENST00000696425.1:c.*370+30G= ENSP00000512620.1:n.*370+30G=
ENST00000696426.1:c.*917+30G= ENSP00000512621.1:n.*917+30G=
ENST00000696427.1:c.*417+30G= ENSP00000512622.1:n.*417+30G=
ENST00000696428.1:c.*1299+30G= ENSP00000512623.1:n.*1299+30G=
ENST00000696429.1:c.1457+30G= ENSP00000512624.1:n.1457+30G=
ENST00000696430.1:c.1457+30G= ENSP00000512625.1:n.1457+30G=
ENST00000393562.10:c.1457+30G= MANE Select ENSP00000377192.3:n.1457+30G=
ENST00000369620.6:c.1595+30G= ENSP00000358633.2:n.1595+30G=
ENST00000393562.6:c.1547+30G= ENSP00000377192.2:n.1547+30G=
ENST00000393564.6:c.1457+30G= ENSP00000377194.2:n.1457+30G=
ENST00000490651.1:n.708G=
ENST00000621232.4:c.1457+30G= ENSP00000483686.1:n.1457+30G=
NM_000402.4:c.1547+30G= NP_000393.4:n.1547+30G=
NM_001042351.2:c.1457+30G= NP_001035810.1:n.1457+30G=
XM_005274657.2:c.1550+30G= XP_005274714.1:n.1550+30G=
XM_005274658.2:c.1460+30G= XP_005274715.1:n.1460+30G=
NM_001360016.2:c.1457+30G= MANE Select NP_001346945.1:n.1457+30G=
NM_001042351.3:c.1457+30G= NP_001035810.1:n.1457+30G=