Canonical Allele Identifier: CA2568376168
Gene: G6PD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154534397dup , CM000685.2:g.154534397dup GRCh38
NC_000023.10:g.153762612dup , CM000685.1:g.153762612dup GRCh37
NC_000023.9:g.153415806dup NCBI36
NG_009015.2:g.18176dup

Transcript Alleles

HGVS Amino-acid change
ENST00000393564.7:c.585dup ENSP00000377194.2:p.Ile196AspfsTer?
ENST00000439227.6:c.588dup ENSP00000395599.2:p.Ile197AspfsTer?
ENST00000696420.1:c.585dup ENSP00000512615.1:p.Ile196AspfsTer?
ENST00000696421.1:c.585dup ENSP00000512616.1:p.Ile196AspfsTer?
ENST00000696422.1:c.448dup
ENST00000696423.1:c.451dup
ENST00000696424.1:c.465dup ENSP00000512619.1:p.Ile156AspfsTer?
ENST00000696425.1:c.585dup ENSP00000512620.1:p.Ile196AspfsTer?
ENST00000696426.1:c.585dup ENSP00000512621.1:p.Ile196AspfsTer?
ENST00000696427.1:c.585dup ENSP00000512622.1:p.Ile196AspfsTer?
ENST00000696428.1:c.*427dup ENSP00000512623.1:n.*427dup
ENST00000696429.1:c.585dup ENSP00000512624.1:p.Ile196AspfsTer?
ENST00000696430.1:c.585dup ENSP00000512625.1:p.Ile196AspfsTer?
ENST00000393562.10:c.585dup MANE Select ENSP00000377192.3:p.Ile196AspfsTer?
ENST00000369620.6:c.585dup ENSP00000358633.2:p.Ile196AspfsTer?
ENST00000393562.6:c.675dup ENSP00000377192.2:p.Ile226AspfsTer?
ENST00000393564.6:c.585dup ENSP00000377194.2:p.Ile196AspfsTer?
ENST00000433845.1:c.585dup ENSP00000394690.1:p.Ile196AspfsTer?
ENST00000439227.5:c.588dup ENSP00000395599.1:p.Ile197AspfsTer?
ENST00000440967.5:c.588dup ENSP00000400648.1:p.Ile197AspfsTer?
ENST00000621232.4:c.585dup ENSP00000483686.1:p.Ile196AspfsTer?
NM_000402.4:c.675dup NP_000393.4:p.Ile226AspfsTer?
NM_001042351.2:c.585dup NP_001035810.1:p.Ile196AspfsTer?
XM_005274657.2:c.678dup XP_005274714.1:p.Ile227AspfsTer?
XM_005274658.2:c.588dup XP_005274715.1:p.Ile197AspfsTer?
XM_011531132.1:c.678dup XP_011529434.1:p.Ile227AspfsTer?
NM_001360016.2:c.585dup MANE Select NP_001346945.1:p.Ile196AspfsTer?
NM_001042351.3:c.585dup NP_001035810.1:p.Ile196AspfsTer?