Canonical Allele Identifier: CA2466724786

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154535909G= , CM000685.2:g.154535909G=	GRCh38
NC_000023.10:g.153764124G= , CM000685.1:g.153764124G=	GRCh37
NC_000023.9:g.153417318G=	NCBI36
NG_009015.2:g.16664C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.267+28C=	ENSP00000377194.2:n.267+28C=
ENST00000439227.6:c.267+28C=	ENSP00000395599.2:n.267+28C=
ENST00000696420.1:c.267+28C=	ENSP00000512615.1:n.267+28C=
ENST00000696421.1:c.267+28C=	ENSP00000512616.1:n.267+28C=
ENST00000696422.1:c.130+45C=
ENST00000696423.1:c.130+45C=
ENST00000696424.1:c.147+28C=	ENSP00000512619.1:n.147+28C=
ENST00000696425.1:c.267+28C=	ENSP00000512620.1:n.267+28C=
ENST00000696426.1:c.267+28C=	ENSP00000512621.1:n.267+28C=
ENST00000696427.1:c.267+28C=	ENSP00000512622.1:n.267+28C=
ENST00000696428.1:c.*109+28C=	ENSP00000512623.1:n.*109+28C=
ENST00000696429.1:c.267+28C=	ENSP00000512624.1:n.267+28C=
ENST00000696430.1:c.267+28C=	ENSP00000512625.1:n.267+28C=
ENST00000696431.1:c.267+28C=	ENSP00000512626.1:n.267+28C=
ENST00000393562.10:c.267+28C= MANE Select	ENSP00000377192.3:n.267+28C=
ENST00000369620.6:c.267+28C=	ENSP00000358633.2:n.267+28C=
ENST00000393562.6:c.357+28C=	ENSP00000377192.2:n.357+28C=
ENST00000393564.6:c.267+28C=	ENSP00000377194.2:n.267+28C=
ENST00000433845.1:c.267+28C=	ENSP00000394690.1:n.267+28C=
ENST00000439227.5:c.267+28C=	ENSP00000395599.1:n.267+28C=
ENST00000440967.5:c.267+28C=	ENSP00000400648.1:n.267+28C=
ENST00000488434.1:n.249C=
ENST00000497281.5:n.221+28C=
ENST00000621232.4:c.267+28C=	ENSP00000483686.1:n.267+28C=
NM_000402.4:c.357+28C=	NP_000393.4:n.357+28C=
NM_001042351.2:c.267+28C=	NP_001035810.1:n.267+28C=
XM_005274657.2:c.357+28C=	XP_005274714.1:n.357+28C=
XM_005274658.2:c.267+28C=	XP_005274715.1:n.267+28C=
XM_011531132.1:c.357+28C=	XP_011529434.1:n.357+28C=
NM_001360016.2:c.267+28C= MANE Select	NP_001346945.1:n.267+28C=
NM_001042351.3:c.267+28C=	NP_001035810.1:n.267+28C=