Canonical Allele Identifier: CA2466722936

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531516_154531517delinsTG , CM000685.2:g.154531516_154531517delinsTG	GRCh38
NC_000023.10:g.153759731_153759732delinsTG , CM000685.1:g.153759731_153759732delinsTG	GRCh37
NC_000023.9:g.153412925_153412926delinsTG	NCBI36
NG_009015.2:g.21056_21057delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.*483_*484delinsCA	ENSP00000377194.2:n.*483_*484delinsCA
ENST00000439227.6:c.*483_*484delinsCA	ENSP00000395599.2:n.*483_*484delinsCA
ENST00000696420.1:c.1457+671_1457+672delinsCA	ENSP00000512615.1:n.1457+671_1457+672delinsCA
ENST00000696421.1:c.1457+671_1457+672delinsCA	ENSP00000512616.1:n.1457+671_1457+672delinsCA
ENST00000696422.1:c.1894_1895delinsCA
ENST00000696423.1:c.1897_1898delinsCA
ENST00000696424.1:c.1883_1884delinsCA	ENSP00000512619.1:n.1883_1884delinsCA
ENST00000696425.1:c.*944_*945delinsCA	ENSP00000512620.1:n.*944_*945delinsCA
ENST00000696426.1:c.*1491_*1492delinsCA	ENSP00000512621.1:n.*1491_*1492delinsCA
ENST00000696427.1:c.*991_*992delinsCA	ENSP00000512622.1:n.*991_*992delinsCA
ENST00000696428.1:c.*1873_*1874delinsCA	ENSP00000512623.1:n.*1873_*1874delinsCA
ENST00000696429.1:c.*483_*484delinsCA	ENSP00000512624.1:n.*483_*484delinsCA
ENST00000696430.1:c.*483_*484delinsCA	ENSP00000512625.1:n.*483_*484delinsCA
ENST00000393562.10:c.*483_*484delinsCA MANE Select	ENSP00000377192.3:n.*483_*484delinsCA
ENST00000393562.6:c.*483_*484delinsCA	ENSP00000377192.2:n.*483_*484delinsCA
ENST00000621232.4:c.*483_*484delinsCA	ENSP00000483686.1:n.*483_*484delinsCA
NM_000402.4:c.*483_*484delinsCA	NP_000393.4:n.*483_*484delinsCA
NM_001042351.2:c.*483_*484delinsCA	NP_001035810.1:n.*483_*484delinsCA
XM_005274657.2:c.*483_*484delinsCA	XP_005274714.1:n.*483_*484delinsCA
XM_005274658.2:c.*483_*484delinsCA	XP_005274715.1:n.*483_*484delinsCA
NM_001360016.2:c.*483_*484delinsCA MANE Select	NP_001346945.1:n.*483_*484delinsCA
NM_001042351.3:c.*483_*484delinsCA	NP_001035810.1:n.*483_*484delinsCA