Canonical Allele Identifier: CA2466723475

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532766T= , CM000685.2:g.154532766T=	GRCh38
NC_000023.10:g.153760981T= , CM000685.1:g.153760981T=	GRCh37
NC_000023.9:g.153414175T=	NCBI36
NG_009015.2:g.19807A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1088A=	ENSP00000377194.2:p.Asn363=
ENST00000439227.6:c.1091A=	ENSP00000395599.2:p.Asn364=
ENST00000696420.1:c.1088A=	ENSP00000512615.1:p.Asn363=
ENST00000696421.1:c.1088A=	ENSP00000512616.1:p.Asn363=
ENST00000696422.1:c.951A=
ENST00000696423.1:c.954A=
ENST00000696424.1:c.940A=	ENSP00000512619.1:n.940A=
ENST00000696425.1:c.*1A=	ENSP00000512620.1:n.*1A=
ENST00000696426.1:c.*548A=	ENSP00000512621.1:n.*548A=
ENST00000696427.1:c.*48A=	ENSP00000512622.1:n.*48A=
ENST00000696428.1:c.*930A=	ENSP00000512623.1:n.*930A=
ENST00000696429.1:c.1088A=	ENSP00000512624.1:p.Asn363=
ENST00000696430.1:c.1088A=	ENSP00000512625.1:p.Asn363=
ENST00000393562.10:c.1088A= MANE Select	ENSP00000377192.3:p.Asn363=
ENST00000369620.6:c.1226A=	ENSP00000358633.2:p.Asn409=
ENST00000393562.6:c.1178A=	ENSP00000377192.2:p.Asn393=
ENST00000393564.6:c.1088A=	ENSP00000377194.2:p.Asn363=
ENST00000490651.1:n.309A=
ENST00000621232.4:c.1088A=	ENSP00000483686.1:p.Asn363=
NM_000402.4:c.1178A=	NP_000393.4:p.Asn393=
NM_001042351.2:c.1088A=	NP_001035810.1:p.Asn363=
XM_005274657.2:c.1181A=	XP_005274714.1:p.Asn394=
XM_005274658.2:c.1091A=	XP_005274715.1:p.Asn364=
XM_011531132.1:c.*1A=	XP_011529434.1:n.*1A=
NM_001360016.2:c.1088A= MANE Select	NP_001346945.1:p.Asn363=
NM_001042351.3:c.1088A=	NP_001035810.1:p.Asn363=