Canonical Allele Identifier: CA519303707

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761308G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533093G>C , CM000685.2:g.154533093G>C	GRCh38
NC_000023.10:g.153761308G>C , CM000685.1:g.153761308G>C	GRCh37
NC_000023.9:g.153414502G>C	NCBI36
NG_009015.2:g.19480C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.900C>G	ENSP00000377194.2:p.Ala300=
ENST00000439227.6:c.903C>G	ENSP00000395599.2:p.Ala301=
ENST00000696420.1:c.900C>G	ENSP00000512615.1:p.Ala300=
ENST00000696421.1:c.900C>G	ENSP00000512616.1:p.Ala300=
ENST00000696422.1:c.763C>G
ENST00000696423.1:c.766C>G
ENST00000696424.1:c.752C>G	ENSP00000512619.1:n.752C>G
ENST00000696425.1:c.865-291C>G	ENSP00000512620.1:n.865-291C>G
ENST00000696426.1:c.*360C>G	ENSP00000512621.1:n.*360C>G
ENST00000696427.1:c.907C>G	ENSP00000512622.1:p.Gln303Glu
ENST00000696428.1:c.*742C>G	ENSP00000512623.1:n.*742C>G
ENST00000696429.1:c.900C>G	ENSP00000512624.1:p.Ala300=
ENST00000696430.1:c.900C>G	ENSP00000512625.1:p.Ala300=
ENST00000393562.10:c.900C>G MANE Select	ENSP00000377192.3:p.Ala300=
ENST00000369620.6:c.1038C>G	ENSP00000358633.2:p.Ala346=
ENST00000393562.6:c.990C>G	ENSP00000377192.2:p.Ala330=
ENST00000393564.6:c.900C>G	ENSP00000377194.2:p.Ala300=
ENST00000439227.5:c.903C>G	ENSP00000395599.1:p.Ala301=
ENST00000440967.5:c.903C>G	ENSP00000400648.1:p.Ala301=
ENST00000621232.4:c.900C>G	ENSP00000483686.1:p.Ala300=
NM_000402.4:c.990C>G	NP_000393.4:p.Ala330=
NM_001042351.2:c.900C>G	NP_001035810.1:p.Ala300=
XM_005274657.2:c.993C>G	XP_005274714.1:p.Ala331=
XM_005274658.2:c.903C>G	XP_005274715.1:p.Ala301=
XM_011531132.1:c.958-291C>G	XP_011529434.1:n.958-291C>G
NM_001360016.2:c.900C>G MANE Select	NP_001346945.1:p.Ala300=
NM_001042351.3:c.900C>G	NP_001035810.1:p.Ala300=