Canonical Allele Identifier: CA415233892

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760822T>G (hg19) ; chrX:g.154532607T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532607T>G , CM000685.2:g.154532607T>G	GRCh38
NC_000023.10:g.153760822T>G , CM000685.1:g.153760822T>G	GRCh37
NC_000023.9:g.153414016T>G	NCBI36
NG_009015.2:g.19966A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.1247A>C	ENSP00000377194.2:p.Glu416Ala
ENST00000439227.6:c.1250A>C	ENSP00000395599.2:p.Glu417Ala
ENST00000696420.1:c.1247A>C	ENSP00000512615.1:p.Glu416Ala
ENST00000696421.1:c.1247A>C	ENSP00000512616.1:p.Glu416Ala
ENST00000696422.1:c.1110A>C
ENST00000696423.1:c.1113A>C
ENST00000696424.1:c.1099A>C	ENSP00000512619.1:n.1099A>C
ENST00000696425.1:c.*160A>C	ENSP00000512620.1:n.*160A>C
ENST00000696426.1:c.*707A>C	ENSP00000512621.1:n.*707A>C
ENST00000696427.1:c.*207A>C	ENSP00000512622.1:n.*207A>C
ENST00000696428.1:c.*1089A>C	ENSP00000512623.1:n.*1089A>C
ENST00000696429.1:c.1247A>C	ENSP00000512624.1:p.Glu416Ala
ENST00000696430.1:c.1247A>C	ENSP00000512625.1:p.Glu416Ala
ENST00000393562.10:c.1247A>C MANE Select	ENSP00000377192.3:p.Glu416Ala
ENST00000369620.6:c.1385A>C	ENSP00000358633.2:p.Glu462Ala
ENST00000393562.6:c.1337A>C	ENSP00000377192.2:p.Glu446Ala
ENST00000393564.6:c.1247A>C	ENSP00000377194.2:p.Glu416Ala
ENST00000490651.1:n.468A>C
ENST00000621232.4:c.1247A>C	ENSP00000483686.1:p.Glu416Ala
NM_000402.4:c.1337A>C	NP_000393.4:p.Glu446Ala
NM_001042351.2:c.1247A>C	NP_001035810.1:p.Glu416Ala
XM_005274657.2:c.1340A>C	XP_005274714.1:p.Glu447Ala
XM_005274658.2:c.1250A>C	XP_005274715.1:p.Glu417Ala
XM_011531132.1:c.*160A>C	XP_011529434.1:n.*160A>C
NM_001360016.2:c.1247A>C MANE Select	NP_001346945.1:p.Glu416Ala
NM_001042351.3:c.1247A>C	NP_001035810.1:p.Glu416Ala