Canonical Allele Identifier: CA2695143509
Gene: G6PD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154532476_154532477dup , CM000685.2:g.154532476_154532477dup GRCh38
NC_000023.10:g.153760691_153760692dup , CM000685.1:g.153760691_153760692dup GRCh37
NC_000023.9:g.153413885_153413886dup NCBI36
NG_009015.2:g.20101_20102dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.1288-10_1288-9dup ENSP00000377194.2:n.1288-10_1288-9dup
ENST00000439227.6:c.1291-10_1291-9dup ENSP00000395599.2:n.1291-10_1291-9dup
ENST00000696420.1:c.1288-10_1288-9dup ENSP00000512615.1:n.1288-10_1288-9dup
ENST00000696421.1:c.1288-10_1288-9dup ENSP00000512616.1:n.1288-10_1288-9dup
ENST00000696422.1:c.1151-10_1151-9dup
ENST00000696423.1:c.1154-10_1154-9dup
ENST00000696424.1:c.1140-10_1140-9dup ENSP00000512619.1:n.1140-10_1140-9dup
ENST00000696425.1:c.*201-10_*201-9dup ENSP00000512620.1:n.*201-10_*201-9dup
ENST00000696426.1:c.*748-10_*748-9dup ENSP00000512621.1:n.*748-10_*748-9dup
ENST00000696427.1:c.*248-10_*248-9dup ENSP00000512622.1:n.*248-10_*248-9dup
ENST00000696428.1:c.*1130-10_*1130-9dup ENSP00000512623.1:n.*1130-10_*1130-9dup
ENST00000696429.1:c.1288-10_1288-9dup ENSP00000512624.1:n.1288-10_1288-9dup
ENST00000696430.1:c.1288-10_1288-9dup ENSP00000512625.1:n.1288-10_1288-9dup
ENST00000393562.10:c.1288-10_1288-9dup MANE Select ENSP00000377192.3:n.1288-10_1288-9dup
ENST00000369620.6:c.1426-10_1426-9dup ENSP00000358633.2:n.1426-10_1426-9dup
ENST00000393562.6:c.1378-10_1378-9dup ENSP00000377192.2:n.1378-10_1378-9dup
ENST00000393564.6:c.1288-10_1288-9dup ENSP00000377194.2:n.1288-10_1288-9dup
ENST00000490651.1:n.509-10_509-9dup
ENST00000621232.4:c.1288-10_1288-9dup ENSP00000483686.1:n.1288-10_1288-9dup
NM_000402.4:c.1378-10_1378-9dup NP_000393.4:n.1378-10_1378-9dup
NM_001042351.2:c.1288-10_1288-9dup NP_001035810.1:n.1288-10_1288-9dup
XM_005274657.2:c.1381-10_1381-9dup XP_005274714.1:n.1381-10_1381-9dup
XM_005274658.2:c.1291-10_1291-9dup XP_005274715.1:n.1291-10_1291-9dup
NM_001360016.2:c.1288-10_1288-9dup MANE Select NP_001346945.1:n.1288-10_1288-9dup
NM_001042351.3:c.1288-10_1288-9dup NP_001035810.1:n.1288-10_1288-9dup