Canonical Allele Identifier: CA2466723645

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533180G= , CM000685.2:g.154533180G=	GRCh38
NC_000023.10:g.153761395G= , CM000685.1:g.153761395G=	GRCh37
NC_000023.9:g.153414589G=	NCBI36
NG_009015.2:g.19393C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.865-52C=	ENSP00000377194.2:n.865-52C=
ENST00000439227.6:c.868-52C=	ENSP00000395599.2:n.868-52C=
ENST00000696420.1:c.865-52C=	ENSP00000512615.1:n.865-52C=
ENST00000696421.1:c.865-52C=	ENSP00000512616.1:n.865-52C=
ENST00000696422.1:c.728-52C=
ENST00000696423.1:c.731-52C=
ENST00000696424.1:c.717-52C=	ENSP00000512619.1:n.717-52C=
ENST00000696425.1:c.865-378C=	ENSP00000512620.1:n.865-378C=
ENST00000696426.1:c.*273C=	ENSP00000512621.1:n.*273C=
ENST00000696427.1:c.872-52C=	ENSP00000512622.1:n.872-52C=
ENST00000696428.1:c.*707-52C=	ENSP00000512623.1:n.*707-52C=
ENST00000696429.1:c.865-52C=	ENSP00000512624.1:n.865-52C=
ENST00000696430.1:c.865-52C=	ENSP00000512625.1:n.865-52C=
ENST00000393562.10:c.865-52C= MANE Select	ENSP00000377192.3:n.865-52C=
ENST00000369620.6:c.1003-52C=	ENSP00000358633.2:n.1003-52C=
ENST00000393562.6:c.955-52C=	ENSP00000377192.2:n.955-52C=
ENST00000393564.6:c.865-52C=	ENSP00000377194.2:n.865-52C=
ENST00000439227.5:c.868-52C=	ENSP00000395599.1:n.868-52C=
ENST00000440967.5:c.868-52C=	ENSP00000400648.1:n.868-52C=
ENST00000621232.4:c.865-52C=	ENSP00000483686.1:n.865-52C=
NM_000402.4:c.955-52C=	NP_000393.4:n.955-52C=
NM_001042351.2:c.865-52C=	NP_001035810.1:n.865-52C=
XM_005274657.2:c.958-52C=	XP_005274714.1:n.958-52C=
XM_005274658.2:c.868-52C=	XP_005274715.1:n.868-52C=
XM_011531132.1:c.958-378C=	XP_011529434.1:n.958-378C=
NM_001360016.2:c.865-52C= MANE Select	NP_001346945.1:n.865-52C=
NM_001042351.3:c.865-52C=	NP_001035810.1:n.865-52C=