Canonical Allele Identifier: CA2539139805

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154534450_154534451insGCG , CM000685.2:g.154534450_154534451insGCG	GRCh38
NC_000023.10:g.153762665_153762666insGCG , CM000685.1:g.153762665_153762666insGCG	GRCh37
NC_000023.9:g.153415859_153415860insGCG	NCBI36
NG_009015.2:g.18123_18124insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.532_533insGCC	ENSP00000377194.2:p.Leu177_Gln178insArg
ENST00000439227.6:c.535_536insGCC	ENSP00000395599.2:p.Leu178_Gln179insArg
ENST00000696420.1:c.532_533insGCC	ENSP00000512615.1:p.Leu177_Gln178insArg
ENST00000696421.1:c.532_533insGCC	ENSP00000512616.1:p.Leu177_Gln178insArg
ENST00000696422.1:c.395_396insGCC
ENST00000696423.1:c.398_399insGCC
ENST00000696424.1:c.412_413insGCC	ENSP00000512619.1:p.Leu137_Gln138insArg
ENST00000696425.1:c.532_533insGCC	ENSP00000512620.1:p.Leu177_Gln178insArg
ENST00000696426.1:c.532_533insGCC	ENSP00000512621.1:p.Leu177_Gln178insArg
ENST00000696427.1:c.532_533insGCC	ENSP00000512622.1:p.Leu177_Gln178insArg
ENST00000696428.1:c.*374_*375insGCC	ENSP00000512623.1:n.*374_*375insGCC
ENST00000696429.1:c.532_533insGCC	ENSP00000512624.1:p.Leu177_Gln178insArg
ENST00000696430.1:c.532_533insGCC	ENSP00000512625.1:p.Leu177_Gln178insArg
ENST00000393562.10:c.532_533insGCC MANE Select	ENSP00000377192.3:p.Leu177_Gln178insArg
ENST00000369620.6:c.532_533insGCC	ENSP00000358633.2:p.Leu177_Gln178insArg
ENST00000393562.6:c.622_623insGCC	ENSP00000377192.2:p.Leu207_Gln208insArg
ENST00000393564.6:c.532_533insGCC	ENSP00000377194.2:p.Leu177_Gln178insArg
ENST00000433845.1:c.532_533insGCC	ENSP00000394690.1:p.Leu177_Gln178insArg
ENST00000439227.5:c.535_536insGCC	ENSP00000395599.1:p.Leu178_Gln179insArg
ENST00000440967.5:c.535_536insGCC	ENSP00000400648.1:p.Leu178_Gln179insArg
ENST00000621232.4:c.532_533insGCC	ENSP00000483686.1:p.Leu177_Gln178insArg
NM_000402.4:c.622_623insGCC	NP_000393.4:p.Leu207_Gln208insArg
NM_001042351.2:c.532_533insGCC	NP_001035810.1:p.Leu177_Gln178insArg
XM_005274657.2:c.625_626insGCC	XP_005274714.1:p.Leu208_Gln209insArg
XM_005274658.2:c.535_536insGCC	XP_005274715.1:p.Leu178_Gln179insArg
XM_011531132.1:c.625_626insGCC	XP_011529434.1:p.Leu208_Gln209insArg
NM_001360016.2:c.532_533insGCC MANE Select	NP_001346945.1:p.Leu177_Gln178insArg
NM_001042351.3:c.532_533insGCC	NP_001035810.1:p.Leu177_Gln178insArg