Canonical Allele Identifier: CA519302949

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760471A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532256A>C , CM000685.2:g.154532256A>C	GRCh38
NC_000023.10:g.153760471A>C , CM000685.1:g.153760471A>C	GRCh37
NC_000023.9:g.153413665A>C	NCBI36
NG_009015.2:g.20317T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.1389T>G	ENSP00000377194.2:p.Arg463=
ENST00000439227.6:c.1392T>G	ENSP00000395599.2:p.Arg464=
ENST00000696420.1:c.1389T>G	ENSP00000512615.1:p.Arg463=
ENST00000696421.1:c.1389T>G	ENSP00000512616.1:p.Arg463=
ENST00000696422.1:c.1252T>G
ENST00000696423.1:c.1255T>G
ENST00000696424.1:c.1241T>G	ENSP00000512619.1:n.1241T>G
ENST00000696425.1:c.*302T>G	ENSP00000512620.1:n.*302T>G
ENST00000696426.1:c.*849T>G	ENSP00000512621.1:n.*849T>G
ENST00000696427.1:c.*349T>G	ENSP00000512622.1:n.*349T>G
ENST00000696428.1:c.*1231T>G	ENSP00000512623.1:n.*1231T>G
ENST00000696429.1:c.1389T>G	ENSP00000512624.1:p.Arg463=
ENST00000696430.1:c.1389T>G	ENSP00000512625.1:p.Arg463=
ENST00000393562.10:c.1389T>G MANE Select	ENSP00000377192.3:p.Arg463=
ENST00000369620.6:c.1527T>G	ENSP00000358633.2:p.Arg509=
ENST00000393562.6:c.1479T>G	ENSP00000377192.2:p.Arg493=
ENST00000393564.6:c.1389T>G	ENSP00000377194.2:p.Arg463=
ENST00000490651.1:n.610T>G
ENST00000621232.4:c.1389T>G	ENSP00000483686.1:p.Arg463=
NM_000402.4:c.1479T>G	NP_000393.4:p.Arg493=
NM_001042351.2:c.1389T>G	NP_001035810.1:p.Arg463=
XM_005274657.2:c.1482T>G	XP_005274714.1:p.Arg494=
XM_005274658.2:c.1392T>G	XP_005274715.1:p.Arg464=
NM_001360016.2:c.1389T>G MANE Select	NP_001346945.1:p.Arg463=
NM_001042351.3:c.1389T>G	NP_001035810.1:p.Arg463=