Canonical Allele Identifier: CA415233732

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760653C>A (hg19) ; chrX:g.154532438C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532438C>A , CM000685.2:g.154532438C>A	GRCh38
NC_000023.10:g.153760653C>A , CM000685.1:g.153760653C>A	GRCh37
NC_000023.9:g.153413847C>A	NCBI36
NG_009015.2:g.20135G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1312G>T	ENSP00000377194.2:p.Glu438Ter
ENST00000439227.6:c.1315G>T	ENSP00000395599.2:p.Glu439Ter
ENST00000696420.1:c.1312G>T	ENSP00000512615.1:p.Glu438Ter
ENST00000696421.1:c.1312G>T	ENSP00000512616.1:p.Glu438Ter
ENST00000696422.1:c.1175G>T
ENST00000696423.1:c.1178G>T
ENST00000696424.1:c.1164G>T	ENSP00000512619.1:n.1164G>T
ENST00000696425.1:c.*225G>T	ENSP00000512620.1:n.*225G>T
ENST00000696426.1:c.*772G>T	ENSP00000512621.1:n.*772G>T
ENST00000696427.1:c.*272G>T	ENSP00000512622.1:n.*272G>T
ENST00000696428.1:c.*1154G>T	ENSP00000512623.1:n.*1154G>T
ENST00000696429.1:c.1312G>T	ENSP00000512624.1:p.Glu438Ter
ENST00000696430.1:c.1312G>T	ENSP00000512625.1:p.Glu438Ter
ENST00000393562.10:c.1312G>T MANE Select	ENSP00000377192.3:p.Glu438Ter
ENST00000369620.6:c.1450G>T	ENSP00000358633.2:p.Glu484Ter
ENST00000393562.6:c.1402G>T	ENSP00000377192.2:p.Glu468Ter
ENST00000393564.6:c.1312G>T	ENSP00000377194.2:p.Glu438Ter
ENST00000490651.1:n.533G>T
ENST00000621232.4:c.1312G>T	ENSP00000483686.1:p.Glu438Ter
NM_000402.4:c.1402G>T	NP_000393.4:p.Glu468Ter
NM_001042351.2:c.1312G>T	NP_001035810.1:p.Glu438Ter
XM_005274657.2:c.1405G>T	XP_005274714.1:p.Glu469Ter
XM_005274658.2:c.1315G>T	XP_005274715.1:p.Glu439Ter
NM_001360016.2:c.1312G>T MANE Select	NP_001346945.1:p.Glu438Ter
NM_001042351.3:c.1312G>T	NP_001035810.1:p.Glu438Ter