Canonical Allele Identifier: CA2695142780

Gene: G6PD

Linked Data

• gnomAD v4: X-154532157-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532160_154532161del , CM000685.2:g.154532160_154532161del	GRCh38
NC_000023.10:g.153760375_153760376del , CM000685.1:g.153760375_153760376del	GRCh37
NC_000023.9:g.153413569_153413570del	NCBI36
NG_009015.2:g.20414_20415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1457+29_1457+30del	ENSP00000377194.2:n.1457+29_1457+30del
ENST00000439227.6:c.1460+29_1460+30del	ENSP00000395599.2:n.1460+29_1460+30del
ENST00000696420.1:c.1457+29_1457+30del	ENSP00000512615.1:n.1457+29_1457+30del
ENST00000696421.1:c.1457+29_1457+30del	ENSP00000512616.1:n.1457+29_1457+30del
ENST00000696422.1:c.1320+29_1320+30del
ENST00000696423.1:c.1323+29_1323+30del
ENST00000696424.1:c.1309+29_1309+30del	ENSP00000512619.1:n.1309+29_1309+30del
ENST00000696425.1:c.*370+29_*370+30del	ENSP00000512620.1:n.*370+29_*370+30del
ENST00000696426.1:c.*917+29_*917+30del	ENSP00000512621.1:n.*917+29_*917+30del
ENST00000696427.1:c.*417+29_*417+30del	ENSP00000512622.1:n.*417+29_*417+30del
ENST00000696428.1:c.*1299+29_*1299+30del	ENSP00000512623.1:n.*1299+29_*1299+30del
ENST00000696429.1:c.1457+29_1457+30del	ENSP00000512624.1:n.1457+29_1457+30del
ENST00000696430.1:c.1457+29_1457+30del	ENSP00000512625.1:n.1457+29_1457+30del
ENST00000393562.10:c.1457+29_1457+30del MANE Select	ENSP00000377192.3:n.1457+29_1457+30del
ENST00000369620.6:c.1595+29_1595+30del	ENSP00000358633.2:n.1595+29_1595+30del
ENST00000393562.6:c.1547+29_1547+30del	ENSP00000377192.2:n.1547+29_1547+30del
ENST00000393564.6:c.1457+29_1457+30del	ENSP00000377194.2:n.1457+29_1457+30del
ENST00000490651.1:n.707_708del
ENST00000621232.4:c.1457+29_1457+30del	ENSP00000483686.1:n.1457+29_1457+30del
NM_000402.4:c.1547+29_1547+30del	NP_000393.4:n.1547+29_1547+30del
NM_001042351.2:c.1457+29_1457+30del	NP_001035810.1:n.1457+29_1457+30del
XM_005274657.2:c.1550+29_1550+30del	XP_005274714.1:n.1550+29_1550+30del
XM_005274658.2:c.1460+29_1460+30del	XP_005274715.1:n.1460+29_1460+30del
NM_001360016.2:c.1457+29_1457+30del MANE Select	NP_001346945.1:n.1457+29_1457+30del
NM_001042351.3:c.1457+29_1457+30del	NP_001035810.1:n.1457+29_1457+30del