Canonical Allele Identifier: CA2695140356

Gene: G6PD

Linked Data

• gnomAD v4: X-154531644-GTCCCTCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531649_154531656del , CM000685.2:g.154531649_154531656del	GRCh38
NC_000023.10:g.153759864_153759871del , CM000685.1:g.153759864_153759871del	GRCh37
NC_000023.9:g.153413058_153413065del	NCBI36
NG_009015.2:g.20921_20928del

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.*348_*355del	ENSP00000377194.2:n.*348_*355del
ENST00000439227.6:c.*348_*355del	ENSP00000395599.2:n.*348_*355del
ENST00000696420.1:c.1457+536_1457+543del	ENSP00000512615.1:n.1457+536_1457+543del
ENST00000696421.1:c.1457+536_1457+543del	ENSP00000512616.1:n.1457+536_1457+543del
ENST00000696422.1:c.1759_1766del
ENST00000696423.1:c.1762_1769del
ENST00000696424.1:c.1748_1755del	ENSP00000512619.1:n.1748_1755del
ENST00000696425.1:c.*809_*816del	ENSP00000512620.1:n.*809_*816del
ENST00000696426.1:c.*1356_*1363del	ENSP00000512621.1:n.*1356_*1363del
ENST00000696427.1:c.*856_*863del	ENSP00000512622.1:n.*856_*863del
ENST00000696428.1:c.*1738_*1745del	ENSP00000512623.1:n.*1738_*1745del
ENST00000696429.1:c.*348_*355del	ENSP00000512624.1:n.*348_*355del
ENST00000696430.1:c.*348_*355del	ENSP00000512625.1:n.*348_*355del
ENST00000393562.10:c.*348_*355del MANE Select	ENSP00000377192.3:n.*348_*355del
ENST00000393562.6:c.*348_*355del	ENSP00000377192.2:n.*348_*355del
ENST00000621232.4:c.*348_*355del	ENSP00000483686.1:n.*348_*355del
NM_000402.4:c.*348_*355del	NP_000393.4:n.*348_*355del
NM_001042351.2:c.*348_*355del	NP_001035810.1:n.*348_*355del
XM_005274657.2:c.*348_*355del	XP_005274714.1:n.*348_*355del
XM_005274658.2:c.*348_*355del	XP_005274715.1:n.*348_*355del
NM_001360016.2:c.*348_*355del MANE Select	NP_001346945.1:n.*348_*355del
NM_001042351.3:c.*348_*355del	NP_001035810.1:n.*348_*355del