Canonical Allele Identifier: CA2695144691

Gene: G6PD

Linked Data

• gnomAD v4: X-154533215-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533215A>C , CM000685.2:g.154533215A>C	GRCh38
NC_000023.10:g.153761430A>C , CM000685.1:g.153761430A>C	GRCh37
NC_000023.9:g.153414624A>C	NCBI36
NG_009015.2:g.19358T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.865-87T>G	ENSP00000377194.2:n.865-87T>G
ENST00000439227.6:c.868-87T>G	ENSP00000395599.2:n.868-87T>G
ENST00000696420.1:c.865-87T>G	ENSP00000512615.1:n.865-87T>G
ENST00000696421.1:c.865-87T>G	ENSP00000512616.1:n.865-87T>G
ENST00000696422.1:c.728-87T>G
ENST00000696423.1:c.731-87T>G
ENST00000696424.1:c.717-87T>G	ENSP00000512619.1:n.717-87T>G
ENST00000696425.1:c.864+361T>G	ENSP00000512620.1:n.864+361T>G
ENST00000696426.1:c.*238T>G	ENSP00000512621.1:n.*238T>G
ENST00000696427.1:c.872-87T>G	ENSP00000512622.1:n.872-87T>G
ENST00000696428.1:c.*707-87T>G	ENSP00000512623.1:n.*707-87T>G
ENST00000696429.1:c.865-87T>G	ENSP00000512624.1:n.865-87T>G
ENST00000696430.1:c.865-87T>G	ENSP00000512625.1:n.865-87T>G
ENST00000393562.10:c.865-87T>G MANE Select	ENSP00000377192.3:n.865-87T>G
ENST00000369620.6:c.1003-87T>G	ENSP00000358633.2:n.1003-87T>G
ENST00000393562.6:c.955-87T>G	ENSP00000377192.2:n.955-87T>G
ENST00000393564.6:c.865-87T>G	ENSP00000377194.2:n.865-87T>G
ENST00000439227.5:c.868-87T>G	ENSP00000395599.1:n.868-87T>G
ENST00000440967.5:c.868-87T>G	ENSP00000400648.1:n.868-87T>G
ENST00000621232.4:c.865-87T>G	ENSP00000483686.1:n.865-87T>G
NM_000402.4:c.955-87T>G	NP_000393.4:n.955-87T>G
NM_001042351.2:c.865-87T>G	NP_001035810.1:n.865-87T>G
XM_005274657.2:c.958-87T>G	XP_005274714.1:n.958-87T>G
XM_005274658.2:c.868-87T>G	XP_005274715.1:n.868-87T>G
XM_011531132.1:c.957+361T>G	XP_011529434.1:n.957+361T>G
NM_001360016.2:c.865-87T>G MANE Select	NP_001346945.1:n.865-87T>G
NM_001042351.3:c.865-87T>G	NP_001035810.1:n.865-87T>G