Canonical Allele Identifier: CA519714534

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760968G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532753G>T , CM000685.2:g.154532753G>T	GRCh38
NC_000023.10:g.153760968G>T , CM000685.1:g.153760968G>T	GRCh37
NC_000023.9:g.153414162G>T	NCBI36
NG_009015.2:g.19820C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.1101C>A	ENSP00000377194.2:p.Ala367=
ENST00000439227.6:c.1104C>A	ENSP00000395599.2:p.Ala368=
ENST00000696420.1:c.1101C>A	ENSP00000512615.1:p.Ala367=
ENST00000696421.1:c.1101C>A	ENSP00000512616.1:p.Ala367=
ENST00000696422.1:c.964C>A
ENST00000696423.1:c.967C>A
ENST00000696424.1:c.953C>A	ENSP00000512619.1:n.953C>A
ENST00000696425.1:c.*14C>A	ENSP00000512620.1:n.*14C>A
ENST00000696426.1:c.*561C>A	ENSP00000512621.1:n.*561C>A
ENST00000696427.1:c.*61C>A	ENSP00000512622.1:n.*61C>A
ENST00000696428.1:c.*943C>A	ENSP00000512623.1:n.*943C>A
ENST00000696429.1:c.1101C>A	ENSP00000512624.1:p.Ala367=
ENST00000696430.1:c.1101C>A	ENSP00000512625.1:p.Ala367=
ENST00000393562.10:c.1101C>A MANE Select	ENSP00000377192.3:p.Ala367=
ENST00000369620.6:c.1239C>A	ENSP00000358633.2:p.Ala413=
ENST00000393562.6:c.1191C>A	ENSP00000377192.2:p.Ala397=
ENST00000393564.6:c.1101C>A	ENSP00000377194.2:p.Ala367=
ENST00000490651.1:n.322C>A
ENST00000621232.4:c.1101C>A	ENSP00000483686.1:p.Ala367=
NM_000402.4:c.1191C>A	NP_000393.4:p.Ala397=
NM_001042351.2:c.1101C>A	NP_001035810.1:p.Ala367=
XM_005274657.2:c.1194C>A	XP_005274714.1:p.Ala398=
XM_005274658.2:c.1104C>A	XP_005274715.1:p.Ala368=
XM_011531132.1:c.*14C>A	XP_011529434.1:n.*14C>A
NM_001360016.2:c.1101C>A MANE Select	NP_001346945.1:p.Ala367=
NM_001042351.3:c.1101C>A	NP_001035810.1:p.Ala367=