Canonical Allele Identifier: CA519302876

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760302T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532087T>C , CM000685.2:g.154532087T>C	GRCh38
NC_000023.10:g.153760302T>C , CM000685.1:g.153760302T>C	GRCh37
NC_000023.9:g.153413496T>C	NCBI36
NG_009015.2:g.20486A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1461A>G	ENSP00000377194.2:p.Arg487=
ENST00000439227.6:c.1464A>G	ENSP00000395599.2:p.Arg488=
ENST00000696420.1:c.1457+101A>G	ENSP00000512615.1:n.1457+101A>G
ENST00000696421.1:c.1457+101A>G	ENSP00000512616.1:n.1457+101A>G
ENST00000696422.1:c.1324A>G
ENST00000696423.1:c.1327A>G
ENST00000696424.1:c.1313A>G	ENSP00000512619.1:n.1313A>G
ENST00000696425.1:c.*374A>G	ENSP00000512620.1:n.*374A>G
ENST00000696426.1:c.*921A>G	ENSP00000512621.1:n.*921A>G
ENST00000696427.1:c.*421A>G	ENSP00000512622.1:n.*421A>G
ENST00000696428.1:c.*1303A>G	ENSP00000512623.1:n.*1303A>G
ENST00000696429.1:c.1461A>G	ENSP00000512624.1:p.Arg487=
ENST00000696430.1:c.1461A>G	ENSP00000512625.1:p.Arg487=
ENST00000393562.10:c.1461A>G MANE Select	ENSP00000377192.3:p.Arg487=
ENST00000369620.6:c.1599A>G	ENSP00000358633.2:p.Arg533=
ENST00000393562.6:c.1551A>G	ENSP00000377192.2:p.Arg517=
ENST00000393564.6:c.1461A>G	ENSP00000377194.2:p.Arg487=
ENST00000490651.1:n.779A>G
ENST00000621232.4:c.1461A>G	ENSP00000483686.1:p.Arg487=
NM_000402.4:c.1551A>G	NP_000393.4:p.Arg517=
NM_001042351.2:c.1461A>G	NP_001035810.1:p.Arg487=
XM_005274657.2:c.1554A>G	XP_005274714.1:p.Arg518=
XM_005274658.2:c.1464A>G	XP_005274715.1:p.Arg488=
NM_001360016.2:c.1461A>G MANE Select	NP_001346945.1:p.Arg487=
NM_001042351.3:c.1461A>G	NP_001035810.1:p.Arg487=