Canonical Allele Identifier: CA2466723274

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532245G= , CM000685.2:g.154532245G=	GRCh38
NC_000023.10:g.153760460G= , CM000685.1:g.153760460G=	GRCh37
NC_000023.9:g.153413654G=	NCBI36
NG_009015.2:g.20328C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.1400C=	ENSP00000377194.2:p.Pro467=
ENST00000439227.6:c.1403C=	ENSP00000395599.2:p.Pro468=
ENST00000696420.1:c.1400C=	ENSP00000512615.1:p.Pro467=
ENST00000696421.1:c.1400C=	ENSP00000512616.1:p.Pro467=
ENST00000696422.1:c.1263C=
ENST00000696423.1:c.1266C=
ENST00000696424.1:c.1252C=	ENSP00000512619.1:n.1252C=
ENST00000696425.1:c.*313C=	ENSP00000512620.1:n.*313C=
ENST00000696426.1:c.*860C=	ENSP00000512621.1:n.*860C=
ENST00000696427.1:c.*360C=	ENSP00000512622.1:n.*360C=
ENST00000696428.1:c.*1242C=	ENSP00000512623.1:n.*1242C=
ENST00000696429.1:c.1400C=	ENSP00000512624.1:p.Pro467=
ENST00000696430.1:c.1400C=	ENSP00000512625.1:p.Pro467=
ENST00000393562.10:c.1400C= MANE Select	ENSP00000377192.3:p.Pro467=
ENST00000369620.6:c.1538C=	ENSP00000358633.2:p.Pro513=
ENST00000393562.6:c.1490C=	ENSP00000377192.2:p.Pro497=
ENST00000393564.6:c.1400C=	ENSP00000377194.2:p.Pro467=
ENST00000490651.1:n.621C=
ENST00000621232.4:c.1400C=	ENSP00000483686.1:p.Pro467=
NM_000402.4:c.1490C=	NP_000393.4:p.Pro497=
NM_001042351.2:c.1400C=	NP_001035810.1:p.Pro467=
XM_005274657.2:c.1493C=	XP_005274714.1:p.Pro498=
XM_005274658.2:c.1403C=	XP_005274715.1:p.Pro468=
NM_001360016.2:c.1400C= MANE Select	NP_001346945.1:p.Pro467=
NM_001042351.3:c.1400C=	NP_001035810.1:p.Pro467=