Canonical Allele Identifier: CA2695140420

Gene: G6PD

Linked Data

• gnomAD v4: X-154531649-T-TCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531652_154531653insACCC , CM000685.2:g.154531652_154531653insACCC	GRCh38
NC_000023.10:g.153759867_153759868insACCC , CM000685.1:g.153759867_153759868insACCC	GRCh37
NC_000023.9:g.153413061_153413062insACCC	NCBI36
NG_009015.2:g.20923_20924insTGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.*350_*351insTGGG	ENSP00000377194.2:n.*350_*351insTGGG
ENST00000439227.6:c.*350_*351insTGGG	ENSP00000395599.2:n.*350_*351insTGGG
ENST00000696420.1:c.1457+538_1457+539insTGGG	ENSP00000512615.1:n.1457+538_1457+539insT...
ENST00000696421.1:c.1457+538_1457+539insTGGG	ENSP00000512616.1:n.1457+538_1457+539insT...
ENST00000696422.1:c.1761_1762insTGGG
ENST00000696423.1:c.1764_1765insTGGG
ENST00000696424.1:c.1750_1751insTGGG	ENSP00000512619.1:n.1750_1751insTGGG
ENST00000696425.1:c.*811_*812insTGGG	ENSP00000512620.1:n.*811_*812insTGGG
ENST00000696426.1:c.*1358_*1359insTGGG	ENSP00000512621.1:n.*1358_*1359insTGGG
ENST00000696427.1:c.*858_*859insTGGG	ENSP00000512622.1:n.*858_*859insTGGG
ENST00000696428.1:c.*1740_*1741insTGGG	ENSP00000512623.1:n.*1740_*1741insTGGG
ENST00000696429.1:c.*350_*351insTGGG	ENSP00000512624.1:n.*350_*351insTGGG
ENST00000696430.1:c.*350_*351insTGGG	ENSP00000512625.1:n.*350_*351insTGGG
ENST00000393562.10:c.*350_*351insTGGG MANE Select	ENSP00000377192.3:n.*350_*351insTGGG
ENST00000393562.6:c.*350_*351insTGGG	ENSP00000377192.2:n.*350_*351insTGGG
ENST00000621232.4:c.*350_*351insTGGG	ENSP00000483686.1:n.*350_*351insTGGG
NM_000402.4:c.*350_*351insTGGG	NP_000393.4:n.*350_*351insTGGG
NM_001042351.2:c.*350_*351insTGGG	NP_001035810.1:n.*350_*351insTGGG
XM_005274657.2:c.*350_*351insTGGG	XP_005274714.1:n.*350_*351insTGGG
XM_005274658.2:c.*350_*351insTGGG	XP_005274715.1:n.*350_*351insTGGG
NM_001360016.2:c.*350_*351insTGGG MANE Select	NP_001346945.1:n.*350_*351insTGGG
NM_001042351.3:c.*350_*351insTGGG	NP_001035810.1:n.*350_*351insTGGG