Canonical Allele Identifier: CA10566001

Gene: G6PD

Linked Data

• dbSNP Id: rs782022518
• ExAC: X:153760380 CCCAGCCCCCACCCTTTCCTCA / C
• MyVariant Identifiers: chrX:g.153760381_153760401del (hg19) ; chrX:g.154532166_154532186del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532168_154532188del , CM000685.2:g.154532168_154532188del	GRCh38
NC_000023.10:g.153760383_153760403del , CM000685.1:g.153760383_153760403del	GRCh37
NC_000023.9:g.153413577_153413597del	NCBI36
NG_009015.2:g.20387_20407del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1457+2_1457+22del
ENST00000439227.6:c.1460+2_1460+22del
ENST00000696420.1:c.1457+2_1457+22del
ENST00000696421.1:c.1457+2_1457+22del
ENST00000696422.1:c.1320+2_1320+22del
ENST00000696423.1:c.1323+2_1323+22del
ENST00000696424.1:c.1309+2_1309+22del
ENST00000696425.1:c.*370+2_*370+22del
ENST00000696426.1:c.*917+2_*917+22del
ENST00000696427.1:c.*417+2_*417+22del
ENST00000696428.1:c.*1299+2_*1299+22del
ENST00000696429.1:c.1457+2_1457+22del
ENST00000696430.1:c.1457+2_1457+22del
ENST00000393562.10:c.1457+2_1457+22del
ENST00000369620.6:c.1595+2_1595+22del
ENST00000393562.6:c.1547+2_1547+22del
ENST00000393564.6:c.1457+2_1457+22del
ENST00000490651.1:n.680_700del
ENST00000621232.4:c.1457+2_1457+22del
NM_000402.4:c.1547+2_1547+22del
NM_001042351.2:c.1457+2_1457+22del
XM_005274657.2:c.1550+2_1550+22del
XM_005274658.2:c.1460+2_1460+22del
NM_001360016.2:c.1457+2_1457+22del
NM_001042351.3:c.1457+2_1457+22del