Canonical Allele Identifier: CA415234924

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761330T>G (hg19) ; chrX:g.154533115T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533115T>G , CM000685.2:g.154533115T>G	GRCh38
NC_000023.10:g.153761330T>G , CM000685.1:g.153761330T>G	GRCh37
NC_000023.9:g.153414524T>G	NCBI36
NG_009015.2:g.19458A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.878A>C	ENSP00000377194.2:p.Lys293Thr
ENST00000439227.6:c.881A>C	ENSP00000395599.2:p.Lys294Thr
ENST00000696420.1:c.878A>C	ENSP00000512615.1:p.Lys293Thr
ENST00000696421.1:c.878A>C	ENSP00000512616.1:p.Lys293Thr
ENST00000696422.1:c.741A>C
ENST00000696423.1:c.744A>C
ENST00000696424.1:c.730A>C	ENSP00000512619.1:n.730A>C
ENST00000696425.1:c.865-313A>C	ENSP00000512620.1:n.865-313A>C
ENST00000696426.1:c.*338A>C	ENSP00000512621.1:n.*338A>C
ENST00000696427.1:c.885A>C	ENSP00000512622.1:p.Glu295Asp
ENST00000696428.1:c.*720A>C	ENSP00000512623.1:n.*720A>C
ENST00000696429.1:c.878A>C	ENSP00000512624.1:p.Lys293Thr
ENST00000696430.1:c.878A>C	ENSP00000512625.1:p.Lys293Thr
ENST00000393562.10:c.878A>C MANE Select	ENSP00000377192.3:p.Lys293Thr
ENST00000369620.6:c.1016A>C	ENSP00000358633.2:p.Lys339Thr
ENST00000393562.6:c.968A>C	ENSP00000377192.2:p.Lys323Thr
ENST00000393564.6:c.878A>C	ENSP00000377194.2:p.Lys293Thr
ENST00000439227.5:c.881A>C	ENSP00000395599.1:p.Lys294Thr
ENST00000440967.5:c.881A>C	ENSP00000400648.1:p.Lys294Thr
ENST00000621232.4:c.878A>C	ENSP00000483686.1:p.Lys293Thr
NM_000402.4:c.968A>C	NP_000393.4:p.Lys323Thr
NM_001042351.2:c.878A>C	NP_001035810.1:p.Lys293Thr
XM_005274657.2:c.971A>C	XP_005274714.1:p.Lys324Thr
XM_005274658.2:c.881A>C	XP_005274715.1:p.Lys294Thr
XM_011531132.1:c.958-313A>C	XP_011529434.1:n.958-313A>C
NM_001360016.2:c.878A>C MANE Select	NP_001346945.1:p.Lys293Thr
NM_001042351.3:c.878A>C	NP_001035810.1:p.Lys293Thr