Canonical Allele Identifier: CA2695140460

Gene: G6PD

Linked Data

• gnomAD v4: X-154531654-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531654_154531655insAA , CM000685.2:g.154531654_154531655insAA	GRCh38
NC_000023.10:g.153759869_153759870insAA , CM000685.1:g.153759869_153759870insAA	GRCh37
NC_000023.9:g.153413063_153413064insAA	NCBI36
NG_009015.2:g.20918_20919insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.*345_*346insTT	ENSP00000377194.2:n.*345_*346insTT
ENST00000439227.6:c.*345_*346insTT	ENSP00000395599.2:n.*345_*346insTT
ENST00000696420.1:c.1457+533_1457+534insTT	ENSP00000512615.1:n.1457+533_1457+534insTT
ENST00000696421.1:c.1457+533_1457+534insTT	ENSP00000512616.1:n.1457+533_1457+534insTT
ENST00000696422.1:c.1756_1757insTT
ENST00000696423.1:c.1759_1760insTT
ENST00000696424.1:c.1745_1746insTT	ENSP00000512619.1:n.1745_1746insTT
ENST00000696425.1:c.*806_*807insTT	ENSP00000512620.1:n.*806_*807insTT
ENST00000696426.1:c.*1353_*1354insTT	ENSP00000512621.1:n.*1353_*1354insTT
ENST00000696427.1:c.*853_*854insTT	ENSP00000512622.1:n.*853_*854insTT
ENST00000696428.1:c.*1735_*1736insTT	ENSP00000512623.1:n.*1735_*1736insTT
ENST00000696429.1:c.*345_*346insTT	ENSP00000512624.1:n.*345_*346insTT
ENST00000696430.1:c.*345_*346insTT	ENSP00000512625.1:n.*345_*346insTT
ENST00000393562.10:c.*345_*346insTT MANE Select	ENSP00000377192.3:n.*345_*346insTT
ENST00000393562.6:c.*345_*346insTT	ENSP00000377192.2:n.*345_*346insTT
ENST00000621232.4:c.*345_*346insTT	ENSP00000483686.1:n.*345_*346insTT
NM_000402.4:c.*345_*346insTT	NP_000393.4:n.*345_*346insTT
NM_001042351.2:c.*345_*346insTT	NP_001035810.1:n.*345_*346insTT
XM_005274657.2:c.*345_*346insTT	XP_005274714.1:n.*345_*346insTT
XM_005274658.2:c.*345_*346insTT	XP_005274715.1:n.*345_*346insTT
NM_001360016.2:c.*345_*346insTT MANE Select	NP_001346945.1:n.*345_*346insTT
NM_001042351.3:c.*345_*346insTT	NP_001035810.1:n.*345_*346insTT