Canonical Allele Identifier: CA415233690

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760632A>T (hg19) ; chrX:g.154532417A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532417A>T , CM000685.2:g.154532417A>T	GRCh38
NC_000023.10:g.153760632A>T , CM000685.1:g.153760632A>T	GRCh37
NC_000023.9:g.153413826A>T	NCBI36
NG_009015.2:g.20156T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.1333T>A	ENSP00000377194.2:p.Phe445Ile
ENST00000439227.6:c.1336T>A	ENSP00000395599.2:p.Phe446Ile
ENST00000696420.1:c.1333T>A	ENSP00000512615.1:p.Phe445Ile
ENST00000696421.1:c.1333T>A	ENSP00000512616.1:p.Phe445Ile
ENST00000696422.1:c.1196T>A
ENST00000696423.1:c.1199T>A
ENST00000696424.1:c.1185T>A	ENSP00000512619.1:n.1185T>A
ENST00000696425.1:c.*246T>A	ENSP00000512620.1:n.*246T>A
ENST00000696426.1:c.*793T>A	ENSP00000512621.1:n.*793T>A
ENST00000696427.1:c.*293T>A	ENSP00000512622.1:n.*293T>A
ENST00000696428.1:c.*1175T>A	ENSP00000512623.1:n.*1175T>A
ENST00000696429.1:c.1333T>A	ENSP00000512624.1:p.Phe445Ile
ENST00000696430.1:c.1333T>A	ENSP00000512625.1:p.Phe445Ile
ENST00000393562.10:c.1333T>A MANE Select	ENSP00000377192.3:p.Phe445Ile
ENST00000369620.6:c.1471T>A	ENSP00000358633.2:p.Phe491Ile
ENST00000393562.6:c.1423T>A	ENSP00000377192.2:p.Phe475Ile
ENST00000393564.6:c.1333T>A	ENSP00000377194.2:p.Phe445Ile
ENST00000490651.1:n.554T>A
ENST00000621232.4:c.1333T>A	ENSP00000483686.1:p.Phe445Ile
NM_000402.4:c.1423T>A	NP_000393.4:p.Phe475Ile
NM_001042351.2:c.1333T>A	NP_001035810.1:p.Phe445Ile
XM_005274657.2:c.1426T>A	XP_005274714.1:p.Phe476Ile
XM_005274658.2:c.1336T>A	XP_005274715.1:p.Phe446Ile
NM_001360016.2:c.1333T>A MANE Select	NP_001346945.1:p.Phe445Ile
NM_001042351.3:c.1333T>A	NP_001035810.1:p.Phe445Ile