Canonical Allele Identifier: CA2466723295

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532306_154532307delinsAG , CM000685.2:g.154532306_154532307delinsAG	GRCh38
NC_000023.10:g.153760521_153760522delinsAG , CM000685.1:g.153760521_153760522delinsAG	GRCh37
NC_000023.9:g.153413715_153413716delinsAG	NCBI36
NG_009015.2:g.20266_20267delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1365-27_1365-26delinsCT	ENSP00000377194.2:n.1365-27_1365-26delinsCT
ENST00000439227.6:c.1368-27_1368-26delinsCT	ENSP00000395599.2:n.1368-27_1368-26delinsCT
ENST00000696420.1:c.1365-27_1365-26delinsCT	ENSP00000512615.1:n.1365-27_1365-26delinsCT
ENST00000696421.1:c.1365-27_1365-26delinsCT	ENSP00000512616.1:n.1365-27_1365-26delinsCT
ENST00000696422.1:c.1228-27_1228-26delinsCT
ENST00000696423.1:c.1231-27_1231-26delinsCT
ENST00000696424.1:c.1217-27_1217-26delinsCT	ENSP00000512619.1:n.1217-27_1217-26delinsCT
ENST00000696425.1:c.*278-27_*278-26delinsCT	ENSP00000512620.1:n.*278-27_*278-26delinsCT
ENST00000696426.1:c.*825-27_*825-26delinsCT	ENSP00000512621.1:n.*825-27_*825-26delinsCT
ENST00000696427.1:c.*325-27_*325-26delinsCT	ENSP00000512622.1:n.*325-27_*325-26delinsCT
ENST00000696428.1:c.*1207-27_*1207-26delinsCT	ENSP00000512623.1:n.*1207-27_*1207-26delinsCT
ENST00000696429.1:c.1365-27_1365-26delinsCT	ENSP00000512624.1:n.1365-27_1365-26delinsCT
ENST00000696430.1:c.1365-27_1365-26delinsCT	ENSP00000512625.1:n.1365-27_1365-26delinsCT
ENST00000393562.10:c.1365-27_1365-26delinsCT MANE Select	ENSP00000377192.3:n.1365-27_1365-26delinsCT
ENST00000369620.6:c.1503-27_1503-26delinsCT	ENSP00000358633.2:n.1503-27_1503-26delinsCT
ENST00000393562.6:c.1455-27_1455-26delinsCT	ENSP00000377192.2:n.1455-27_1455-26delinsCT
ENST00000393564.6:c.1365-27_1365-26delinsCT	ENSP00000377194.2:n.1365-27_1365-26delinsCT
ENST00000490651.1:n.586-27_586-26delinsCT
ENST00000621232.4:c.1365-27_1365-26delinsCT	ENSP00000483686.1:n.1365-27_1365-26delinsCT
NM_000402.4:c.1455-27_1455-26delinsCT	NP_000393.4:n.1455-27_1455-26delinsCT
NM_001042351.2:c.1365-27_1365-26delinsCT	NP_001035810.1:n.1365-27_1365-26delinsCT
XM_005274657.2:c.1458-27_1458-26delinsCT	XP_005274714.1:n.1458-27_1458-26delinsCT
XM_005274658.2:c.1368-27_1368-26delinsCT	XP_005274715.1:n.1368-27_1368-26delinsCT
NM_001360016.2:c.1365-27_1365-26delinsCT MANE Select	NP_001346945.1:n.1365-27_1365-26delinsCT
NM_001042351.3:c.1365-27_1365-26delinsCT	NP_001035810.1:n.1365-27_1365-26delinsCT