Canonical Allele Identifier: CA10565990

Gene: G6PD

Linked Data

• dbSNP Id: rs782488219
• ExAC: X:153760352 A / C
• gnomAD v2: X-153760352-A-C
• gnomAD v3: X-154532137-A-C
• gnomAD v4: X-154532137-A-C
• MyVariant Identifiers: chrX:g.153760352A>C (hg19) ; chrX:g.154532137A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532137A>C , CM000685.2:g.154532137A>C	GRCh38
NC_000023.10:g.153760352A>C , CM000685.1:g.153760352A>C	GRCh37
NC_000023.9:g.153413546A>C	NCBI36
NG_009015.2:g.20436T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1458-47T>G	ENSP00000377194.2:n.1458-47T>G
ENST00000439227.6:c.1461-47T>G	ENSP00000395599.2:n.1461-47T>G
ENST00000696420.1:c.1457+51T>G	ENSP00000512615.1:n.1457+51T>G
ENST00000696421.1:c.1457+51T>G	ENSP00000512616.1:n.1457+51T>G
ENST00000696422.1:c.1321-47T>G
ENST00000696423.1:c.1324-47T>G
ENST00000696424.1:c.1310-47T>G	ENSP00000512619.1:n.1310-47T>G
ENST00000696425.1:c.*371-47T>G	ENSP00000512620.1:n.*371-47T>G
ENST00000696426.1:c.*918-47T>G	ENSP00000512621.1:n.*918-47T>G
ENST00000696427.1:c.*418-47T>G	ENSP00000512622.1:n.*418-47T>G
ENST00000696428.1:c.*1300-47T>G	ENSP00000512623.1:n.*1300-47T>G
ENST00000696429.1:c.1458-47T>G	ENSP00000512624.1:n.1458-47T>G
ENST00000696430.1:c.1458-47T>G	ENSP00000512625.1:n.1458-47T>G
ENST00000393562.10:c.1458-47T>G MANE Select	ENSP00000377192.3:n.1458-47T>G
ENST00000369620.6:c.1596-47T>G	ENSP00000358633.2:n.1596-47T>G
ENST00000393562.6:c.1548-47T>G	ENSP00000377192.2:n.1548-47T>G
ENST00000393564.6:c.1458-47T>G	ENSP00000377194.2:n.1458-47T>G
ENST00000490651.1:n.729T>G
ENST00000621232.4:c.1458-47T>G	ENSP00000483686.1:n.1458-47T>G
NM_000402.4:c.1548-47T>G	NP_000393.4:n.1548-47T>G
NM_001042351.2:c.1458-47T>G	NP_001035810.1:n.1458-47T>G
XM_005274657.2:c.1551-47T>G	XP_005274714.1:n.1551-47T>G
XM_005274658.2:c.1461-47T>G	XP_005274715.1:n.1461-47T>G
NM_001360016.2:c.1458-47T>G MANE Select	NP_001346945.1:n.1458-47T>G
NM_001042351.3:c.1458-47T>G	NP_001035810.1:n.1458-47T>G