Canonical Allele Identifier: CA645291576

Gene: G6PD

Linked Data

• dbSNP Id: rs199970830
• gnomAD v2: X-153761359-G-C
• gnomAD v4: X-154533144-G-C
• MyVariant Identifiers: chrX:g.153761359G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533144G>C , CM000685.2:g.154533144G>C	GRCh38
NC_000023.10:g.153761359G>C , CM000685.1:g.153761359G>C	GRCh37
NC_000023.9:g.153414553G>C	NCBI36
NG_009015.2:g.19429C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.865-16C>G	ENSP00000377194.2:n.865-16C>G
ENST00000439227.6:c.868-16C>G	ENSP00000395599.2:n.868-16C>G
ENST00000696420.1:c.865-16C>G	ENSP00000512615.1:n.865-16C>G
ENST00000696421.1:c.865-16C>G	ENSP00000512616.1:n.865-16C>G
ENST00000696422.1:c.728-16C>G
ENST00000696423.1:c.731-16C>G
ENST00000696424.1:c.717-16C>G	ENSP00000512619.1:n.717-16C>G
ENST00000696425.1:c.865-342C>G	ENSP00000512620.1:n.865-342C>G
ENST00000696426.1:c.*309C>G	ENSP00000512621.1:n.*309C>G
ENST00000696427.1:c.872-16C>G	ENSP00000512622.1:n.872-16C>G
ENST00000696428.1:c.*707-16C>G	ENSP00000512623.1:n.*707-16C>G
ENST00000696429.1:c.865-16C>G	ENSP00000512624.1:n.865-16C>G
ENST00000696430.1:c.865-16C>G	ENSP00000512625.1:n.865-16C>G
ENST00000393562.10:c.865-16C>G MANE Select	ENSP00000377192.3:n.865-16C>G
ENST00000369620.6:c.1003-16C>G	ENSP00000358633.2:n.1003-16C>G
ENST00000393562.6:c.955-16C>G	ENSP00000377192.2:n.955-16C>G
ENST00000393564.6:c.865-16C>G	ENSP00000377194.2:n.865-16C>G
ENST00000439227.5:c.868-16C>G	ENSP00000395599.1:n.868-16C>G
ENST00000440967.5:c.868-16C>G	ENSP00000400648.1:n.868-16C>G
ENST00000621232.4:c.865-16C>G	ENSP00000483686.1:n.865-16C>G
NM_000402.4:c.955-16C>G	NP_000393.4:n.955-16C>G
NM_001042351.2:c.865-16C>G	NP_001035810.1:n.865-16C>G
XM_005274657.2:c.958-16C>G	XP_005274714.1:n.958-16C>G
XM_005274658.2:c.868-16C>G	XP_005274715.1:n.868-16C>G
XM_011531132.1:c.958-342C>G	XP_011529434.1:n.958-342C>G
NM_001360016.2:c.865-16C>G MANE Select	NP_001346945.1:n.865-16C>G
NM_001042351.3:c.865-16C>G	NP_001035810.1:n.865-16C>G