Canonical Allele Identifier: CA415234565

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761247C>G (hg19) ; chrX:g.154533032C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533032C>G , CM000685.2:g.154533032C>G	GRCh38
NC_000023.10:g.153761247C>G , CM000685.1:g.153761247C>G	GRCh37
NC_000023.9:g.153414441C>G	NCBI36
NG_009015.2:g.19541G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.961G>C	ENSP00000377194.2:p.Gly321Arg
ENST00000439227.6:c.964G>C	ENSP00000395599.2:p.Gly322Arg
ENST00000696420.1:c.961G>C	ENSP00000512615.1:p.Gly321Arg
ENST00000696421.1:c.961G>C	ENSP00000512616.1:p.Gly321Arg
ENST00000696422.1:c.824G>C
ENST00000696423.1:c.827G>C
ENST00000696424.1:c.813G>C	ENSP00000512619.1:n.813G>C
ENST00000696425.1:c.865-230G>C	ENSP00000512620.1:n.865-230G>C
ENST00000696426.1:c.*421G>C	ENSP00000512621.1:n.*421G>C
ENST00000696427.1:c.968G>C	ENSP00000512622.1:p.Arg323Thr
ENST00000696428.1:c.*803G>C	ENSP00000512623.1:n.*803G>C
ENST00000696429.1:c.961G>C	ENSP00000512624.1:p.Gly321Arg
ENST00000696430.1:c.961G>C	ENSP00000512625.1:p.Gly321Arg
ENST00000393562.10:c.961G>C MANE Select	ENSP00000377192.3:p.Gly321Arg
ENST00000369620.6:c.1099G>C	ENSP00000358633.2:p.Gly367Arg
ENST00000393562.6:c.1051G>C	ENSP00000377192.2:p.Gly351Arg
ENST00000393564.6:c.961G>C	ENSP00000377194.2:p.Gly321Arg
ENST00000439227.5:c.964G>C	ENSP00000395599.1:p.Gly322Arg
ENST00000490651.1:n.43G>C
ENST00000621232.4:c.961G>C	ENSP00000483686.1:p.Gly321Arg
NM_000402.4:c.1051G>C	NP_000393.4:p.Gly351Arg
NM_001042351.2:c.961G>C	NP_001035810.1:p.Gly321Arg
XM_005274657.2:c.1054G>C	XP_005274714.1:p.Gly352Arg
XM_005274658.2:c.964G>C	XP_005274715.1:p.Gly322Arg
XM_011531132.1:c.958-230G>C	XP_011529434.1:n.958-230G>C
NM_001360016.2:c.961G>C MANE Select	NP_001346945.1:p.Gly321Arg
NM_001042351.3:c.961G>C	NP_001035810.1:p.Gly321Arg