Canonical Allele Identifier: CA415231767

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760229G>C (hg19) ; chrX:g.154532014G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532014G>C , CM000685.2:g.154532014G>C	GRCh38
NC_000023.10:g.153760229G>C , CM000685.1:g.153760229G>C	GRCh37
NC_000023.9:g.153413423G>C	NCBI36
NG_009015.2:g.20559C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1534C>G	ENSP00000377194.2:p.Pro512Ala
ENST00000439227.6:c.1537C>G	ENSP00000395599.2:p.Pro513Ala
ENST00000696420.1:c.1457+174C>G	ENSP00000512615.1:n.1457+174C>G
ENST00000696421.1:c.1457+174C>G	ENSP00000512616.1:n.1457+174C>G
ENST00000696422.1:c.1397C>G
ENST00000696423.1:c.1400C>G
ENST00000696424.1:c.1386C>G	ENSP00000512619.1:n.1386C>G
ENST00000696425.1:c.*447C>G	ENSP00000512620.1:n.*447C>G
ENST00000696426.1:c.*994C>G	ENSP00000512621.1:n.*994C>G
ENST00000696427.1:c.*494C>G	ENSP00000512622.1:n.*494C>G
ENST00000696428.1:c.*1376C>G	ENSP00000512623.1:n.*1376C>G
ENST00000696429.1:c.1534C>G	ENSP00000512624.1:p.Pro512Ala
ENST00000696430.1:c.1534C>G	ENSP00000512625.1:p.Pro512Ala
ENST00000393562.10:c.1534C>G MANE Select	ENSP00000377192.3:p.Pro512Ala
ENST00000369620.6:c.1672C>G	ENSP00000358633.2:p.Pro558Ala
ENST00000393562.6:c.1624C>G	ENSP00000377192.2:p.Pro542Ala
ENST00000393564.6:c.1534C>G	ENSP00000377194.2:p.Pro512Ala
ENST00000621232.4:c.1534C>G	ENSP00000483686.1:p.Pro512Ala
NM_000402.4:c.1624C>G	NP_000393.4:p.Pro542Ala
NM_001042351.2:c.1534C>G	NP_001035810.1:p.Pro512Ala
XM_005274657.2:c.1627C>G	XP_005274714.1:p.Pro543Ala
XM_005274658.2:c.1537C>G	XP_005274715.1:p.Pro513Ala
NM_001360016.2:c.1534C>G MANE Select	NP_001346945.1:p.Pro512Ala
NM_001042351.3:c.1534C>G	NP_001035810.1:p.Pro512Ala