Canonical Allele Identifier: CA2466724171
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154534414G= , CM000685.2:g.154534414G= GRCh38
NC_000023.10:g.153762629G= , CM000685.1:g.153762629G= GRCh37
NC_000023.9:g.153415823G= NCBI36
NG_009015.2:g.18159C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.568C= ENSP00000377194.2:p.Leu190=
ENST00000439227.6:c.571C= ENSP00000395599.2:p.Leu191=
ENST00000696420.1:c.568C= ENSP00000512615.1:p.Leu190=
ENST00000696421.1:c.568C= ENSP00000512616.1:p.Leu190=
ENST00000696422.1:c.431C=
ENST00000696423.1:c.434C=
ENST00000696424.1:c.448C= ENSP00000512619.1:p.Leu150=
ENST00000696425.1:c.568C= ENSP00000512620.1:p.Leu190=
ENST00000696426.1:c.568C= ENSP00000512621.1:p.Leu190=
ENST00000696427.1:c.568C= ENSP00000512622.1:p.Leu190=
ENST00000696428.1:c.*410C= ENSP00000512623.1:n.*410C=
ENST00000696429.1:c.568C= ENSP00000512624.1:p.Leu190=
ENST00000696430.1:c.568C= ENSP00000512625.1:p.Leu190=
ENST00000393562.10:c.568C= MANE Select ENSP00000377192.3:p.Leu190=
ENST00000369620.6:c.568C= ENSP00000358633.2:p.Leu190=
ENST00000393562.6:c.658C= ENSP00000377192.2:p.Leu220=
ENST00000393564.6:c.568C= ENSP00000377194.2:p.Leu190=
ENST00000433845.1:c.568C= ENSP00000394690.1:p.Leu190=
ENST00000439227.5:c.571C= ENSP00000395599.1:p.Leu191=
ENST00000440967.5:c.571C= ENSP00000400648.1:p.Leu191=
ENST00000621232.4:c.568C= ENSP00000483686.1:p.Leu190=
NM_000402.4:c.658C= NP_000393.4:p.Leu220=
NM_001042351.2:c.568C= NP_001035810.1:p.Leu190=
XM_005274657.2:c.661C= XP_005274714.1:p.Leu221=
XM_005274658.2:c.571C= XP_005274715.1:p.Leu191=
XM_011531132.1:c.661C= XP_011529434.1:p.Leu221=
NM_001360016.2:c.568C= MANE Select NP_001346945.1:p.Leu190=
NM_001042351.3:c.568C= NP_001035810.1:p.Leu190=