Canonical Allele Identifier: CA415234268

Gene: G6PD

Linked Data

• ClinVar Variation Id: 1722610
• ClinVar RCV Id: RCV002305720
• dbSNP Id: rs2148328996
• MyVariant Identifiers: chrX:g.153760988C>T (hg19) ; chrX:g.154532773C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532773C>T , CM000685.2:g.154532773C>T	GRCh38
NC_000023.10:g.153760988C>T , CM000685.1:g.153760988C>T	GRCh37
NC_000023.9:g.153414182C>T	NCBI36
NG_009015.2:g.19800G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1081G>A	ENSP00000377194.2:p.Ala361Thr
ENST00000439227.6:c.1084G>A	ENSP00000395599.2:p.Ala362Thr
ENST00000696420.1:c.1081G>A	ENSP00000512615.1:p.Ala361Thr
ENST00000696421.1:c.1081G>A	ENSP00000512616.1:p.Ala361Thr
ENST00000696422.1:c.944G>A
ENST00000696423.1:c.947G>A
ENST00000696424.1:c.933G>A	ENSP00000512619.1:n.933G>A
ENST00000696425.1:c.894G>A	ENSP00000512620.1:p.Arg298=
ENST00000696426.1:c.*541G>A	ENSP00000512621.1:n.*541G>A
ENST00000696427.1:c.*41G>A	ENSP00000512622.1:n.*41G>A
ENST00000696428.1:c.*923G>A	ENSP00000512623.1:n.*923G>A
ENST00000696429.1:c.1081G>A	ENSP00000512624.1:p.Ala361Thr
ENST00000696430.1:c.1081G>A	ENSP00000512625.1:p.Ala361Thr
ENST00000393562.10:c.1081G>A MANE Select	ENSP00000377192.3:p.Ala361Thr
ENST00000369620.6:c.1219G>A	ENSP00000358633.2:p.Ala407Thr
ENST00000393562.6:c.1171G>A	ENSP00000377192.2:p.Ala391Thr
ENST00000393564.6:c.1081G>A	ENSP00000377194.2:p.Ala361Thr
ENST00000490651.1:n.302G>A
ENST00000621232.4:c.1081G>A	ENSP00000483686.1:p.Ala361Thr
NM_000402.4:c.1171G>A	NP_000393.4:p.Ala391Thr
NM_001042351.2:c.1081G>A	NP_001035810.1:p.Ala361Thr
XM_005274657.2:c.1174G>A	XP_005274714.1:p.Ala392Thr
XM_005274658.2:c.1084G>A	XP_005274715.1:p.Ala362Thr
XM_011531132.1:c.987G>A	XP_011529434.1:p.Arg329=
NM_001360016.2:c.1081G>A MANE Select	NP_001346945.1:p.Ala361Thr
NM_001042351.3:c.1081G>A	NP_001035810.1:p.Ala361Thr