Canonical Allele Identifier: CA415232569

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760466A>G (hg19) ; chrX:g.154532251A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532251A>G , CM000685.2:g.154532251A>G	GRCh38
NC_000023.10:g.153760466A>G , CM000685.1:g.153760466A>G	GRCh37
NC_000023.9:g.153413660A>G	NCBI36
NG_009015.2:g.20322T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.1394T>C	ENSP00000377194.2:p.Phe465Ser
ENST00000439227.6:c.1397T>C	ENSP00000395599.2:p.Phe466Ser
ENST00000696420.1:c.1394T>C	ENSP00000512615.1:p.Phe465Ser
ENST00000696421.1:c.1394T>C	ENSP00000512616.1:p.Phe465Ser
ENST00000696422.1:c.1257T>C
ENST00000696423.1:c.1260T>C
ENST00000696424.1:c.1246T>C	ENSP00000512619.1:n.1246T>C
ENST00000696425.1:c.*307T>C	ENSP00000512620.1:n.*307T>C
ENST00000696426.1:c.*854T>C	ENSP00000512621.1:n.*854T>C
ENST00000696427.1:c.*354T>C	ENSP00000512622.1:n.*354T>C
ENST00000696428.1:c.*1236T>C	ENSP00000512623.1:n.*1236T>C
ENST00000696429.1:c.1394T>C	ENSP00000512624.1:p.Phe465Ser
ENST00000696430.1:c.1394T>C	ENSP00000512625.1:p.Phe465Ser
ENST00000393562.10:c.1394T>C MANE Select	ENSP00000377192.3:p.Phe465Ser
ENST00000369620.6:c.1532T>C	ENSP00000358633.2:p.Phe511Ser
ENST00000393562.6:c.1484T>C	ENSP00000377192.2:p.Phe495Ser
ENST00000393564.6:c.1394T>C	ENSP00000377194.2:p.Phe465Ser
ENST00000490651.1:n.615T>C
ENST00000621232.4:c.1394T>C	ENSP00000483686.1:p.Phe465Ser
NM_000402.4:c.1484T>C	NP_000393.4:p.Phe495Ser
NM_001042351.2:c.1394T>C	NP_001035810.1:p.Phe465Ser
XM_005274657.2:c.1487T>C	XP_005274714.1:p.Phe496Ser
XM_005274658.2:c.1397T>C	XP_005274715.1:p.Phe466Ser
NM_001360016.2:c.1394T>C MANE Select	NP_001346945.1:p.Phe465Ser
NM_001042351.3:c.1394T>C	NP_001035810.1:p.Phe465Ser