Canonical Allele Identifier: CA415234026

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760879T>G (hg19) ; chrX:g.154532664T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532664T>G , CM000685.2:g.154532664T>G	GRCh38
NC_000023.10:g.153760879T>G , CM000685.1:g.153760879T>G	GRCh37
NC_000023.9:g.153414073T>G	NCBI36
NG_009015.2:g.19909A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.1190A>C	ENSP00000377194.2:p.Asn397Thr
ENST00000439227.6:c.1193A>C	ENSP00000395599.2:p.Asn398Thr
ENST00000696420.1:c.1190A>C	ENSP00000512615.1:p.Asn397Thr
ENST00000696421.1:c.1190A>C	ENSP00000512616.1:p.Asn397Thr
ENST00000696422.1:c.1053A>C
ENST00000696423.1:c.1056A>C
ENST00000696424.1:c.1042A>C	ENSP00000512619.1:n.1042A>C
ENST00000696425.1:c.*103A>C	ENSP00000512620.1:n.*103A>C
ENST00000696426.1:c.*650A>C	ENSP00000512621.1:n.*650A>C
ENST00000696427.1:c.*150A>C	ENSP00000512622.1:n.*150A>C
ENST00000696428.1:c.*1032A>C	ENSP00000512623.1:n.*1032A>C
ENST00000696429.1:c.1190A>C	ENSP00000512624.1:p.Asn397Thr
ENST00000696430.1:c.1190A>C	ENSP00000512625.1:p.Asn397Thr
ENST00000393562.10:c.1190A>C MANE Select	ENSP00000377192.3:p.Asn397Thr
ENST00000369620.6:c.1328A>C	ENSP00000358633.2:p.Asn443Thr
ENST00000393562.6:c.1280A>C	ENSP00000377192.2:p.Asn427Thr
ENST00000393564.6:c.1190A>C	ENSP00000377194.2:p.Asn397Thr
ENST00000490651.1:n.411A>C
ENST00000621232.4:c.1190A>C	ENSP00000483686.1:p.Asn397Thr
NM_000402.4:c.1280A>C	NP_000393.4:p.Asn427Thr
NM_001042351.2:c.1190A>C	NP_001035810.1:p.Asn397Thr
XM_005274657.2:c.1283A>C	XP_005274714.1:p.Asn428Thr
XM_005274658.2:c.1193A>C	XP_005274715.1:p.Asn398Thr
XM_011531132.1:c.*103A>C	XP_011529434.1:n.*103A>C
NM_001360016.2:c.1190A>C MANE Select	NP_001346945.1:p.Asn397Thr
NM_001042351.3:c.1190A>C	NP_001035810.1:p.Asn397Thr