Canonical Allele Identifier: CA2695140434

Gene: G6PD

Linked Data

• gnomAD v4: X-154531650-CCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531653_154531655del , CM000685.2:g.154531653_154531655del	GRCh38
NC_000023.10:g.153759868_153759870del , CM000685.1:g.153759868_153759870del	GRCh37
NC_000023.9:g.153413062_153413064del	NCBI36
NG_009015.2:g.20920_20922del

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.*347_*349del	ENSP00000377194.2:n.*347_*349del
ENST00000439227.6:c.*347_*349del	ENSP00000395599.2:n.*347_*349del
ENST00000696420.1:c.1457+535_1457+537del	ENSP00000512615.1:n.1457+535_1457+537del
ENST00000696421.1:c.1457+535_1457+537del	ENSP00000512616.1:n.1457+535_1457+537del
ENST00000696422.1:c.1758_1760del
ENST00000696423.1:c.1761_1763del
ENST00000696424.1:c.1747_1749del	ENSP00000512619.1:n.1747_1749del
ENST00000696425.1:c.*808_*810del	ENSP00000512620.1:n.*808_*810del
ENST00000696426.1:c.*1355_*1357del	ENSP00000512621.1:n.*1355_*1357del
ENST00000696427.1:c.*855_*857del	ENSP00000512622.1:n.*855_*857del
ENST00000696428.1:c.*1737_*1739del	ENSP00000512623.1:n.*1737_*1739del
ENST00000696429.1:c.*347_*349del	ENSP00000512624.1:n.*347_*349del
ENST00000696430.1:c.*347_*349del	ENSP00000512625.1:n.*347_*349del
ENST00000393562.10:c.*347_*349del MANE Select	ENSP00000377192.3:n.*347_*349del
ENST00000393562.6:c.*347_*349del	ENSP00000377192.2:n.*347_*349del
ENST00000621232.4:c.*347_*349del	ENSP00000483686.1:n.*347_*349del
NM_000402.4:c.*347_*349del	NP_000393.4:n.*347_*349del
NM_001042351.2:c.*347_*349del	NP_001035810.1:n.*347_*349del
XM_005274657.2:c.*347_*349del	XP_005274714.1:n.*347_*349del
XM_005274658.2:c.*347_*349del	XP_005274715.1:n.*347_*349del
NM_001360016.2:c.*347_*349del MANE Select	NP_001346945.1:n.*347_*349del
NM_001042351.3:c.*347_*349del	NP_001035810.1:n.*347_*349del