Canonical Allele Identifier: CA2695140384
Gene: G6PD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154531645_154531646insACCA , CM000685.2:g.154531645_154531646insACCA GRCh38
NC_000023.10:g.153759860_153759861insACCA , CM000685.1:g.153759860_153759861insACCA GRCh37
NC_000023.9:g.153413054_153413055insACCA NCBI36
NG_009015.2:g.20927_20928insTGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000393564.7:c.*354_*355insTGGT ENSP00000377194.2:n.*354_*355insTGGT
ENST00000439227.6:c.*354_*355insTGGT ENSP00000395599.2:n.*354_*355insTGGT
ENST00000696420.1:c.1457+542_1457+543insTGGT ENSP00000512615.1:n.1457+542_1457+543insT...
ENST00000696421.1:c.1457+542_1457+543insTGGT ENSP00000512616.1:n.1457+542_1457+543insT...
ENST00000696422.1:c.1765_1766insTGGT
ENST00000696423.1:c.1768_1769insTGGT
ENST00000696424.1:c.1754_1755insTGGT ENSP00000512619.1:n.1754_1755insTGGT
ENST00000696425.1:c.*815_*816insTGGT ENSP00000512620.1:n.*815_*816insTGGT
ENST00000696426.1:c.*1362_*1363insTGGT ENSP00000512621.1:n.*1362_*1363insTGGT
ENST00000696427.1:c.*862_*863insTGGT ENSP00000512622.1:n.*862_*863insTGGT
ENST00000696428.1:c.*1744_*1745insTGGT ENSP00000512623.1:n.*1744_*1745insTGGT
ENST00000696429.1:c.*354_*355insTGGT ENSP00000512624.1:n.*354_*355insTGGT
ENST00000696430.1:c.*354_*355insTGGT ENSP00000512625.1:n.*354_*355insTGGT
ENST00000393562.10:c.*354_*355insTGGT MANE Select ENSP00000377192.3:n.*354_*355insTGGT
ENST00000393562.6:c.*354_*355insTGGT ENSP00000377192.2:n.*354_*355insTGGT
ENST00000621232.4:c.*354_*355insTGGT ENSP00000483686.1:n.*354_*355insTGGT
NM_000402.4:c.*354_*355insTGGT NP_000393.4:n.*354_*355insTGGT
NM_001042351.2:c.*354_*355insTGGT NP_001035810.1:n.*354_*355insTGGT
XM_005274657.2:c.*354_*355insTGGT XP_005274714.1:n.*354_*355insTGGT
XM_005274658.2:c.*354_*355insTGGT XP_005274715.1:n.*354_*355insTGGT
NM_001360016.2:c.*354_*355insTGGT MANE Select NP_001346945.1:n.*354_*355insTGGT
NM_001042351.3:c.*354_*355insTGGT NP_001035810.1:n.*354_*355insTGGT