Canonical Allele Identifier: CA2466723590
Gene: G6PD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154533012_154533036delinsCGTGGGGTCGTCCAGGTACCCTTTG , CM000685.2:g.154533012_154533036delinsCGTGGGGTCGTCCAGGTACCCTTTG GRCh38
NC_000023.10:g.153761227_153761251delinsCGTGGGGTCGTCCAGGTACCCTTTG , CM000685.1:g.153761227_153761251delinsCGTGGGGTCGTCCAGGTACCCTTTG GRCh37
NC_000023.9:g.153414421_153414445delinsCGTGGGGTCGTCCAGGTACCCTTTG NCBI36
NG_009015.2:g.19537_19561delinsCAAAGGGTACCTGGACGACCCCACG

Transcript Alleles

HGVS Amino-acid change
ENST00000393564.7:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000377194.2:p.Thr319=
ENST00000439227.6:c.960_984delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000395599.2:p.Thr320=
ENST00000696420.1:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000512615.1:p.Thr319=
ENST00000696421.1:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000512616.1:p.Thr319=
ENST00000696422.1:c.820_844delinsCAAAGGGTACCTGGACGACCCCACG
ENST00000696423.1:c.823_847delinsCAAAGGGTACCTGGACGACCCCACG
ENST00000696424.1:c.809_833delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000512619.1:n.809_833delinsCAAAGGGT...
ENST00000696425.1:c.865-234_865-210delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000512620.1:n.865-234_865-210delins...
ENST00000696426.1:c.*417_*441delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000512621.1:n.*417_*441delinsCAAAGG...
ENST00000696427.1:c.964_988delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000512622.1:p.Gln322=
ENST00000696428.1:c.*799_*823delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000512623.1:n.*799_*823delinsCAAAGG...
ENST00000696429.1:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000512624.1:p.Thr319=
ENST00000696430.1:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000512625.1:p.Thr319=
ENST00000393562.10:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG MANE Select ENSP00000377192.3:p.Thr319=
ENST00000369620.6:c.1095_1119delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000358633.2:p.Thr365=
ENST00000393562.6:c.1047_1071delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000377192.2:p.Thr349=
ENST00000393564.6:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000377194.2:p.Thr319=
ENST00000439227.5:c.960_984delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000395599.1:p.Thr320=
ENST00000490651.1:n.39_63delinsCAAAGGGTACCTGGACGACCCCACG
ENST00000621232.4:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG ENSP00000483686.1:p.Thr319=
NM_000402.4:c.1047_1071delinsCAAAGGGTACCTGGACGACCCCACG NP_000393.4:p.Thr349=
NM_001042351.2:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG NP_001035810.1:p.Thr319=
XM_005274657.2:c.1050_1074delinsCAAAGGGTACCTGGACGACCCCACG XP_005274714.1:p.Thr350=
XM_005274658.2:c.960_984delinsCAAAGGGTACCTGGACGACCCCACG XP_005274715.1:p.Thr320=
XM_011531132.1:c.958-234_958-210delinsCAAAGGGTACCTGGACGACCCCACG XP_011529434.1:n.958-234_958-210delinsCAA...
NM_001360016.2:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG MANE Select NP_001346945.1:p.Thr319=
NM_001042351.3:c.957_981delinsCAAAGGGTACCTGGACGACCCCACG NP_001035810.1:p.Thr319=