Canonical Allele Identifier: CA2522576334

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154534419_154534420insGA , CM000685.2:g.154534419_154534420insGA	GRCh38
NC_000023.10:g.153762634_153762635insGA , CM000685.1:g.153762634_153762635insGA	GRCh37
NC_000023.9:g.153415828_153415829insGA	NCBI36
NG_009015.2:g.18153_18154insTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.562_563insTC	ENSP00000377194.2:p.Ser188PhefsTer28
ENST00000439227.6:c.565_566insTC	ENSP00000395599.2:p.Ser189PhefsTer28
ENST00000696420.1:c.562_563insTC	ENSP00000512615.1:p.Ser188PhefsTer28
ENST00000696421.1:c.562_563insTC	ENSP00000512616.1:p.Ser188PhefsTer28
ENST00000696422.1:c.425_426insTC
ENST00000696423.1:c.428_429insTC
ENST00000696424.1:c.442_443insTC	ENSP00000512619.1:p.Ser148PhefsTer28
ENST00000696425.1:c.562_563insTC	ENSP00000512620.1:p.Ser188PhefsTer28
ENST00000696426.1:c.562_563insTC	ENSP00000512621.1:p.Ser188PhefsTer28
ENST00000696427.1:c.562_563insTC	ENSP00000512622.1:p.Ser188PhefsTer28
ENST00000696428.1:c.*404_*405insTC	ENSP00000512623.1:n.*404_*405insTC
ENST00000696429.1:c.562_563insTC	ENSP00000512624.1:p.Ser188PhefsTer28
ENST00000696430.1:c.562_563insTC	ENSP00000512625.1:p.Ser188PhefsTer28
ENST00000393562.10:c.562_563insTC MANE Select	ENSP00000377192.3:p.Ser188PhefsTer28
ENST00000369620.6:c.562_563insTC	ENSP00000358633.2:p.Ser188PhefsTer28
ENST00000393562.6:c.652_653insTC	ENSP00000377192.2:p.Ser218PhefsTer28
ENST00000393564.6:c.562_563insTC	ENSP00000377194.2:p.Ser188PhefsTer28
ENST00000433845.1:c.562_563insTC	ENSP00000394690.1:p.Ser188PhefsTer28
ENST00000439227.5:c.565_566insTC	ENSP00000395599.1:p.Ser189PhefsTer28
ENST00000440967.5:c.565_566insTC	ENSP00000400648.1:p.Ser189PhefsTer28
ENST00000621232.4:c.562_563insTC	ENSP00000483686.1:p.Ser188PhefsTer28
NM_000402.4:c.652_653insTC	NP_000393.4:p.Ser218PhefsTer28
NM_001042351.2:c.562_563insTC	NP_001035810.1:p.Ser188PhefsTer28
XM_005274657.2:c.655_656insTC	XP_005274714.1:p.Ser219PhefsTer28
XM_005274658.2:c.565_566insTC	XP_005274715.1:p.Ser189PhefsTer28
XM_011531132.1:c.655_656insTC	XP_011529434.1:p.Ser219PhefsTer28
NM_001360016.2:c.562_563insTC MANE Select	NP_001346945.1:p.Ser188PhefsTer28
NM_001042351.3:c.562_563insTC	NP_001035810.1:p.Ser188PhefsTer28