Canonical Allele Identifier: CA415234015

Gene: G6PD

Linked Data

• dbSNP Id: rs868963994
• gnomAD v2: X-153760874-C-T
• gnomAD v4: X-154532659-C-T
• MyVariant Identifiers: chrX:g.153760874C>T (hg19) ; chrX:g.154532659C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532659C>T , CM000685.2:g.154532659C>T	GRCh38
NC_000023.10:g.153760874C>T , CM000685.1:g.153760874C>T	GRCh37
NC_000023.9:g.153414068C>T	NCBI36
NG_009015.2:g.19914G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1195G>A	ENSP00000377194.2:p.Ala399Thr
ENST00000439227.6:c.1198G>A	ENSP00000395599.2:p.Ala400Thr
ENST00000696420.1:c.1195G>A	ENSP00000512615.1:p.Ala399Thr
ENST00000696421.1:c.1195G>A	ENSP00000512616.1:p.Ala399Thr
ENST00000696422.1:c.1058G>A
ENST00000696423.1:c.1061G>A
ENST00000696424.1:c.1047G>A	ENSP00000512619.1:n.1047G>A
ENST00000696425.1:c.*108G>A	ENSP00000512620.1:n.*108G>A
ENST00000696426.1:c.*655G>A	ENSP00000512621.1:n.*655G>A
ENST00000696427.1:c.*155G>A	ENSP00000512622.1:n.*155G>A
ENST00000696428.1:c.*1037G>A	ENSP00000512623.1:n.*1037G>A
ENST00000696429.1:c.1195G>A	ENSP00000512624.1:p.Ala399Thr
ENST00000696430.1:c.1195G>A	ENSP00000512625.1:p.Ala399Thr
ENST00000393562.10:c.1195G>A MANE Select	ENSP00000377192.3:p.Ala399Thr
ENST00000369620.6:c.1333G>A	ENSP00000358633.2:p.Ala445Thr
ENST00000393562.6:c.1285G>A	ENSP00000377192.2:p.Ala429Thr
ENST00000393564.6:c.1195G>A	ENSP00000377194.2:p.Ala399Thr
ENST00000490651.1:n.416G>A
ENST00000621232.4:c.1195G>A	ENSP00000483686.1:p.Ala399Thr
NM_000402.4:c.1285G>A	NP_000393.4:p.Ala429Thr
NM_001042351.2:c.1195G>A	NP_001035810.1:p.Ala399Thr
XM_005274657.2:c.1288G>A	XP_005274714.1:p.Ala430Thr
XM_005274658.2:c.1198G>A	XP_005274715.1:p.Ala400Thr
XM_011531132.1:c.*108G>A	XP_011529434.1:n.*108G>A
NM_001360016.2:c.1195G>A MANE Select	NP_001346945.1:p.Ala399Thr
NM_001042351.3:c.1195G>A	NP_001035810.1:p.Ala399Thr