Canonical Allele Identifier: CA2695140411

Gene: G6PD

Linked Data

• gnomAD v4: X-154531648-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531648_154531649insA , CM000685.2:g.154531648_154531649insA	GRCh38
NC_000023.10:g.153759863_153759864insA , CM000685.1:g.153759863_153759864insA	GRCh37
NC_000023.9:g.153413057_153413058insA	NCBI36
NG_009015.2:g.20924_20925insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.*351_*352insT	ENSP00000377194.2:n.*351_*352insT
ENST00000439227.6:c.*351_*352insT	ENSP00000395599.2:n.*351_*352insT
ENST00000696420.1:c.1457+539_1457+540insT	ENSP00000512615.1:n.1457+539_1457+540insT...
ENST00000696421.1:c.1457+539_1457+540insT	ENSP00000512616.1:n.1457+539_1457+540insT...
ENST00000696422.1:c.1762_1763insT
ENST00000696423.1:c.1765_1766insT
ENST00000696424.1:c.1751_1752insT	ENSP00000512619.1:n.1751_1752insT
ENST00000696425.1:c.*812_*813insT	ENSP00000512620.1:n.*812_*813insT
ENST00000696426.1:c.*1359_*1360insT	ENSP00000512621.1:n.*1359_*1360insT
ENST00000696427.1:c.*859_*860insT	ENSP00000512622.1:n.*859_*860insT
ENST00000696428.1:c.*1741_*1742insT	ENSP00000512623.1:n.*1741_*1742insT
ENST00000696429.1:c.*351_*352insT	ENSP00000512624.1:n.*351_*352insT
ENST00000696430.1:c.*351_*352insT	ENSP00000512625.1:n.*351_*352insT
ENST00000393562.10:c.*351_*352insT MANE Select	ENSP00000377192.3:n.*351_*352insT
ENST00000393562.6:c.*351_*352insT	ENSP00000377192.2:n.*351_*352insT
ENST00000621232.4:c.*351_*352insT	ENSP00000483686.1:n.*351_*352insT
NM_000402.4:c.*351_*352insT	NP_000393.4:n.*351_*352insT
NM_001042351.2:c.*351_*352insT	NP_001035810.1:n.*351_*352insT
XM_005274657.2:c.*351_*352insT	XP_005274714.1:n.*351_*352insT
XM_005274658.2:c.*351_*352insT	XP_005274715.1:n.*351_*352insT
NM_001360016.2:c.*351_*352insT MANE Select	NP_001346945.1:n.*351_*352insT
NM_001042351.3:c.*351_*352insT	NP_001035810.1:n.*351_*352insT