Canonical Allele Identifier: CA2466723560
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154532963_154532965delinsCAT , CM000685.2:g.154532963_154532965delinsCAT GRCh38
NC_000023.10:g.153761178_153761180delinsCAT , CM000685.1:g.153761178_153761180delinsCAT GRCh37
NC_000023.9:g.153414372_153414374delinsCAT NCBI36
NG_009015.2:g.19608_19610delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.1028_1030delinsATG ENSP00000377194.2:p.Tyr343=
ENST00000439227.6:c.1031_1033delinsATG ENSP00000395599.2:p.Tyr344=
ENST00000696420.1:c.1028_1030delinsATG ENSP00000512615.1:p.Tyr343=
ENST00000696421.1:c.1028_1030delinsATG ENSP00000512616.1:p.Tyr343=
ENST00000696422.1:c.891_893delinsATG
ENST00000696423.1:c.894_896delinsATG
ENST00000696424.1:c.880_882delinsATG ENSP00000512619.1:n.880_882delinsATG
ENST00000696425.1:c.865-163_865-161delinsATG ENSP00000512620.1:n.865-163_865-161delinsATG
ENST00000696426.1:c.*488_*490delinsATG ENSP00000512621.1:n.*488_*490delinsATG
ENST00000696427.1:c.1035_1037delinsATG ENSP00000512622.1:p.Leu345=
ENST00000696428.1:c.*870_*872delinsATG ENSP00000512623.1:n.*870_*872delinsATG
ENST00000696429.1:c.1028_1030delinsATG ENSP00000512624.1:p.Tyr343=
ENST00000696430.1:c.1028_1030delinsATG ENSP00000512625.1:p.Tyr343=
ENST00000393562.10:c.1028_1030delinsATG MANE Select ENSP00000377192.3:p.Tyr343=
ENST00000369620.6:c.1166_1168delinsATG ENSP00000358633.2:p.Tyr389=
ENST00000393562.6:c.1118_1120delinsATG ENSP00000377192.2:p.Tyr373=
ENST00000393564.6:c.1028_1030delinsATG ENSP00000377194.2:p.Tyr343=
ENST00000490651.1:n.110_112delinsATG
ENST00000621232.4:c.1028_1030delinsATG ENSP00000483686.1:p.Tyr343=
NM_000402.4:c.1118_1120delinsATG NP_000393.4:p.Tyr373=
NM_001042351.2:c.1028_1030delinsATG NP_001035810.1:p.Tyr343=
XM_005274657.2:c.1121_1123delinsATG XP_005274714.1:p.Tyr374=
XM_005274658.2:c.1031_1033delinsATG XP_005274715.1:p.Tyr344=
XM_011531132.1:c.958-163_958-161delinsATG XP_011529434.1:n.958-163_958-161delinsATG
NM_001360016.2:c.1028_1030delinsATG MANE Select NP_001346945.1:p.Tyr343=
NM_001042351.3:c.1028_1030delinsATG NP_001035810.1:p.Tyr343=