Canonical Allele Identifier: CA415234957

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761339T>A (hg19) ; chrX:g.154533124T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533124T>A , CM000685.2:g.154533124T>A	GRCh38
NC_000023.10:g.153761339T>A , CM000685.1:g.153761339T>A	GRCh37
NC_000023.9:g.153414533T>A	NCBI36
NG_009015.2:g.19449A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.869A>T	ENSP00000377194.2:p.Lys290Met
ENST00000439227.6:c.872A>T	ENSP00000395599.2:p.Lys291Met
ENST00000696420.1:c.869A>T	ENSP00000512615.1:p.Lys290Met
ENST00000696421.1:c.869A>T	ENSP00000512616.1:p.Lys290Met
ENST00000696422.1:c.732A>T
ENST00000696423.1:c.735A>T
ENST00000696424.1:c.721A>T	ENSP00000512619.1:p.Arg241Trp
ENST00000696425.1:c.865-322A>T	ENSP00000512620.1:n.865-322A>T
ENST00000696426.1:c.*329A>T	ENSP00000512621.1:n.*329A>T
ENST00000696427.1:c.876A>T	ENSP00000512622.1:p.Gln292His
ENST00000696428.1:c.*711A>T	ENSP00000512623.1:n.*711A>T
ENST00000696429.1:c.869A>T	ENSP00000512624.1:p.Lys290Met
ENST00000696430.1:c.869A>T	ENSP00000512625.1:p.Lys290Met
ENST00000393562.10:c.869A>T MANE Select	ENSP00000377192.3:p.Lys290Met
ENST00000369620.6:c.1007A>T	ENSP00000358633.2:p.Lys336Met
ENST00000393562.6:c.959A>T	ENSP00000377192.2:p.Lys320Met
ENST00000393564.6:c.869A>T	ENSP00000377194.2:p.Lys290Met
ENST00000439227.5:c.872A>T	ENSP00000395599.1:p.Lys291Met
ENST00000440967.5:c.872A>T	ENSP00000400648.1:p.Lys291Met
ENST00000621232.4:c.869A>T	ENSP00000483686.1:p.Lys290Met
NM_000402.4:c.959A>T	NP_000393.4:p.Lys320Met
NM_001042351.2:c.869A>T	NP_001035810.1:p.Lys290Met
XM_005274657.2:c.962A>T	XP_005274714.1:p.Lys321Met
XM_005274658.2:c.872A>T	XP_005274715.1:p.Lys291Met
XM_011531132.1:c.958-322A>T	XP_011529434.1:n.958-322A>T
NM_001360016.2:c.869A>T MANE Select	NP_001346945.1:p.Lys290Met
NM_001042351.3:c.869A>T	NP_001035810.1:p.Lys290Met