Canonical Allele Identifier: CA2508004126

Gene: G6PD

Linked Data

• gnomAD v4: X-154531642-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531643del , CM000685.2:g.154531643del	GRCh38
NG_009015.2:g.20930del

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.*357del	ENSP00000377194.2:n.*357del
ENST00000439227.6:c.*357del	ENSP00000395599.2:n.*357del
ENST00000696420.1:c.1457+545del	ENSP00000512615.1:n.1457+545del
ENST00000696421.1:c.1457+545del	ENSP00000512616.1:n.1457+545del
ENST00000696422.1:c.1768del
ENST00000696423.1:c.1771del
ENST00000696424.1:c.1757del	ENSP00000512619.1:n.1757del
ENST00000696425.1:c.*818del	ENSP00000512620.1:n.*818del
ENST00000696426.1:c.*1365del	ENSP00000512621.1:n.*1365del
ENST00000696427.1:c.*865del	ENSP00000512622.1:n.*865del
ENST00000696428.1:c.*1747del	ENSP00000512623.1:n.*1747del
ENST00000696429.1:c.*357del	ENSP00000512624.1:n.*357del
ENST00000696430.1:c.*357del	ENSP00000512625.1:n.*357del
ENST00000393562.10:c.*357del MANE Select	ENSP00000377192.3:n.*357del
ENST00000393562.6:c.*357del	ENSP00000377192.2:n.*357del
ENST00000621232.4:c.*357del	ENSP00000483686.1:n.*357del
NM_000402.4:c.*357del	NP_000393.4:n.*357del
NM_001042351.2:c.*357del	NP_001035810.1:n.*357del
XM_005274657.2:c.*357del	XP_005274714.1:n.*357del
XM_005274658.2:c.*357del	XP_005274715.1:n.*357del
NM_001360016.2:c.*357del MANE Select	NP_001346945.1:n.*357del
NM_001042351.3:c.*357del	NP_001035810.1:n.*357del