Canonical Allele Identifier: CA2695140388

Gene: G6PD

Linked Data

• gnomAD v4: X-154531645-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531645_154531646insG , CM000685.2:g.154531645_154531646insG	GRCh38
NC_000023.10:g.153759860_153759861insG , CM000685.1:g.153759860_153759861insG	GRCh37
NC_000023.9:g.153413054_153413055insG	NCBI36
NG_009015.2:g.20927_20928insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.*354_*355insC	ENSP00000377194.2:n.*354_*355insC
ENST00000439227.6:c.*354_*355insC	ENSP00000395599.2:n.*354_*355insC
ENST00000696420.1:c.1457+542_1457+543insC	ENSP00000512615.1:n.1457+542_1457+543insC...
ENST00000696421.1:c.1457+542_1457+543insC	ENSP00000512616.1:n.1457+542_1457+543insC...
ENST00000696422.1:c.1765_1766insC
ENST00000696423.1:c.1768_1769insC
ENST00000696424.1:c.1754_1755insC	ENSP00000512619.1:n.1754_1755insC
ENST00000696425.1:c.*815_*816insC	ENSP00000512620.1:n.*815_*816insC
ENST00000696426.1:c.*1362_*1363insC	ENSP00000512621.1:n.*1362_*1363insC
ENST00000696427.1:c.*862_*863insC	ENSP00000512622.1:n.*862_*863insC
ENST00000696428.1:c.*1744_*1745insC	ENSP00000512623.1:n.*1744_*1745insC
ENST00000696429.1:c.*354_*355insC	ENSP00000512624.1:n.*354_*355insC
ENST00000696430.1:c.*354_*355insC	ENSP00000512625.1:n.*354_*355insC
ENST00000393562.10:c.*354_*355insC MANE Select	ENSP00000377192.3:n.*354_*355insC
ENST00000393562.6:c.*354_*355insC	ENSP00000377192.2:n.*354_*355insC
ENST00000621232.4:c.*354_*355insC	ENSP00000483686.1:n.*354_*355insC
NM_000402.4:c.*354_*355insC	NP_000393.4:n.*354_*355insC
NM_001042351.2:c.*354_*355insC	NP_001035810.1:n.*354_*355insC
XM_005274657.2:c.*354_*355insC	XP_005274714.1:n.*354_*355insC
XM_005274658.2:c.*354_*355insC	XP_005274715.1:n.*354_*355insC
NM_001360016.2:c.*354_*355insC MANE Select	NP_001346945.1:n.*354_*355insC
NM_001042351.3:c.*354_*355insC	NP_001035810.1:n.*354_*355insC