Canonical Allele Identifier: CA10566107
Gene: G6PD HGNC NCBI

Linked Data

dbSNP Id: rs782587403

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154533045G>A , CM000685.2:g.154533045G>A GRCh38
NC_000023.10:g.153761260G>A , CM000685.1:g.153761260G>A GRCh37
NC_000023.9:g.153414454G>A NCBI36
NG_009015.2:g.19528C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.948C>T ENSP00000377194.2:p.Gly316=
ENST00000439227.6:c.951C>T ENSP00000395599.2:p.Gly317=
ENST00000696420.1:c.948C>T ENSP00000512615.1:p.Gly316=
ENST00000696421.1:c.948C>T ENSP00000512616.1:p.Gly316=
ENST00000696422.1:c.811C>T
ENST00000696423.1:c.814C>T
ENST00000696424.1:c.800C>T ENSP00000512619.1:n.800C>T
ENST00000696425.1:c.865-243C>T ENSP00000512620.1:n.865-243C>T
ENST00000696426.1:c.*408C>T ENSP00000512621.1:n.*408C>T
ENST00000696427.1:c.955C>T ENSP00000512622.1:p.Arg319Ter
ENST00000696428.1:c.*790C>T ENSP00000512623.1:n.*790C>T
ENST00000696429.1:c.948C>T ENSP00000512624.1:p.Gly316=
ENST00000696430.1:c.948C>T ENSP00000512625.1:p.Gly316=
ENST00000393562.10:c.948C>T MANE Select ENSP00000377192.3:p.Gly316=
ENST00000369620.6:c.1086C>T ENSP00000358633.2:p.Gly362=
ENST00000393562.6:c.1038C>T ENSP00000377192.2:p.Gly346=
ENST00000393564.6:c.948C>T ENSP00000377194.2:p.Gly316=
ENST00000439227.5:c.951C>T ENSP00000395599.1:p.Gly317=
ENST00000440967.5:c.951C>T ENSP00000400648.1:p.Gly317=
ENST00000490651.1:n.30C>T
ENST00000621232.4:c.948C>T ENSP00000483686.1:p.Gly316=
NM_000402.4:c.1038C>T NP_000393.4:p.Gly346=
NM_001042351.2:c.948C>T NP_001035810.1:p.Gly316=
XM_005274657.2:c.1041C>T XP_005274714.1:p.Gly347=
XM_005274658.2:c.951C>T XP_005274715.1:p.Gly317=
XM_011531132.1:c.958-243C>T XP_011529434.1:n.958-243C>T
NM_001360016.2:c.948C>T MANE Select NP_001346945.1:p.Gly316=
NM_001042351.3:c.948C>T NP_001035810.1:p.Gly316=