Canonical Allele Identifier: CA415235415

Gene: G6PD

Linked Data

• gnomAD v4: X-154533662-T-C
• MyVariant Identifiers: chrX:g.153761877T>C (hg19) ; chrX:g.154533662T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533662T>C , CM000685.2:g.154533662T>C	GRCh38
NC_000023.10:g.153761877T>C , CM000685.1:g.153761877T>C	GRCh37
NC_000023.9:g.153415071T>C	NCBI36
NG_009015.2:g.18911A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.778A>G	ENSP00000377194.2:p.Met260Val
ENST00000439227.6:c.781A>G	ENSP00000395599.2:p.Met261Val
ENST00000696420.1:c.778A>G	ENSP00000512615.1:p.Met260Val
ENST00000696421.1:c.778A>G	ENSP00000512616.1:p.Met260Val
ENST00000696422.1:c.641A>G
ENST00000696423.1:c.644A>G
ENST00000696424.1:c.651-21A>G	ENSP00000512619.1:n.651-21A>G
ENST00000696425.1:c.778A>G	ENSP00000512620.1:p.Met260Val
ENST00000696426.1:c.778A>G	ENSP00000512621.1:p.Met260Val
ENST00000696427.1:c.778A>G	ENSP00000512622.1:p.Met260Val
ENST00000696428.1:c.*620A>G	ENSP00000512623.1:n.*620A>G
ENST00000696429.1:c.778A>G	ENSP00000512624.1:p.Met260Val
ENST00000696430.1:c.778A>G	ENSP00000512625.1:p.Met260Val
ENST00000393562.10:c.778A>G MANE Select	ENSP00000377192.3:p.Met260Val
ENST00000369620.6:c.916A>G	ENSP00000358633.2:p.Met306Val
ENST00000393562.6:c.868A>G	ENSP00000377192.2:p.Met290Val
ENST00000393564.6:c.778A>G	ENSP00000377194.2:p.Met260Val
ENST00000439227.5:c.781A>G	ENSP00000395599.1:p.Met261Val
ENST00000440967.5:c.781A>G	ENSP00000400648.1:p.Met261Val
ENST00000489497.1:n.167A>G
ENST00000621232.4:c.778A>G	ENSP00000483686.1:p.Met260Val
NM_000402.4:c.868A>G	NP_000393.4:p.Met290Val
NM_001042351.2:c.778A>G	NP_001035810.1:p.Met260Val
XM_005274657.2:c.871A>G	XP_005274714.1:p.Met291Val
XM_005274658.2:c.781A>G	XP_005274715.1:p.Met261Val
XM_011531132.1:c.871A>G	XP_011529434.1:p.Met291Val
NM_001360016.2:c.778A>G MANE Select	NP_001346945.1:p.Met260Val
NM_001042351.3:c.778A>G	NP_001035810.1:p.Met260Val