Canonical Allele Identifier: CA2695145029

Gene: G6PD

Linked Data

• gnomAD v4: X-154533467-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533467T>C , CM000685.2:g.154533467T>C	GRCh38
NC_000023.10:g.153761682T>C , CM000685.1:g.153761682T>C	GRCh37
NC_000023.9:g.153414876T>C	NCBI36
NG_009015.2:g.19106A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.864+109A>G	ENSP00000377194.2:n.864+109A>G
ENST00000439227.6:c.867+109A>G	ENSP00000395599.2:n.867+109A>G
ENST00000696420.1:c.864+109A>G	ENSP00000512615.1:n.864+109A>G
ENST00000696421.1:c.864+109A>G	ENSP00000512616.1:n.864+109A>G
ENST00000696422.1:c.727+109A>G
ENST00000696423.1:c.730+109A>G
ENST00000696424.1:c.716+109A>G	ENSP00000512619.1:n.716+109A>G
ENST00000696425.1:c.864+109A>G	ENSP00000512620.1:n.864+109A>G
ENST00000696426.1:c.889A>G	ENSP00000512621.1:p.Ser297Gly
ENST00000696427.1:c.871+102A>G	ENSP00000512622.1:n.871+102A>G
ENST00000696428.1:c.*706+109A>G	ENSP00000512623.1:n.*706+109A>G
ENST00000696429.1:c.864+109A>G	ENSP00000512624.1:n.864+109A>G
ENST00000696430.1:c.864+109A>G	ENSP00000512625.1:n.864+109A>G
ENST00000393562.10:c.864+109A>G MANE Select	ENSP00000377192.3:n.864+109A>G
ENST00000369620.6:c.1002+109A>G	ENSP00000358633.2:n.1002+109A>G
ENST00000393562.6:c.954+109A>G	ENSP00000377192.2:n.954+109A>G
ENST00000393564.6:c.864+109A>G	ENSP00000377194.2:n.864+109A>G
ENST00000439227.5:c.867+109A>G	ENSP00000395599.1:n.867+109A>G
ENST00000440967.5:c.867+109A>G	ENSP00000400648.1:n.867+109A>G
ENST00000489497.1:n.362A>G
ENST00000621232.4:c.864+109A>G	ENSP00000483686.1:n.864+109A>G
NM_000402.4:c.954+109A>G	NP_000393.4:n.954+109A>G
NM_001042351.2:c.864+109A>G	NP_001035810.1:n.864+109A>G
XM_005274657.2:c.957+109A>G	XP_005274714.1:n.957+109A>G
XM_005274658.2:c.867+109A>G	XP_005274715.1:n.867+109A>G
XM_011531132.1:c.957+109A>G	XP_011529434.1:n.957+109A>G
NM_001360016.2:c.864+109A>G MANE Select	NP_001346945.1:n.864+109A>G
NM_001042351.3:c.864+109A>G	NP_001035810.1:n.864+109A>G