Canonical Allele Identifier: CA2695139721

Gene: G6PD

Linked Data

• gnomAD v4: X-154531510-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531510A>C , CM000685.2:g.154531510A>C	GRCh38
NC_000023.10:g.153759725A>C , CM000685.1:g.153759725A>C	GRCh37
NC_000023.9:g.153412919A>C	NCBI36
NG_009015.2:g.21063T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.*490T>G	ENSP00000377194.2:n.*490T>G
ENST00000439227.6:c.*490T>G	ENSP00000395599.2:n.*490T>G
ENST00000696420.1:c.1457+678T>G	ENSP00000512615.1:n.1457+678T>G
ENST00000696421.1:c.1457+678T>G	ENSP00000512616.1:n.1457+678T>G
ENST00000696422.1:c.1901T>G
ENST00000696423.1:c.1904T>G
ENST00000696424.1:c.1890T>G	ENSP00000512619.1:n.1890T>G
ENST00000696425.1:c.*951T>G	ENSP00000512620.1:n.*951T>G
ENST00000696426.1:c.*1498T>G	ENSP00000512621.1:n.*1498T>G
ENST00000696427.1:c.*998T>G	ENSP00000512622.1:n.*998T>G
ENST00000696428.1:c.*1880T>G	ENSP00000512623.1:n.*1880T>G
ENST00000696429.1:c.*490T>G	ENSP00000512624.1:n.*490T>G
ENST00000696430.1:c.*490T>G	ENSP00000512625.1:n.*490T>G
ENST00000393562.10:c.*490T>G MANE Select	ENSP00000377192.3:n.*490T>G
ENST00000393562.6:c.*490T>G	ENSP00000377192.2:n.*490T>G
ENST00000621232.4:c.*490T>G	ENSP00000483686.1:n.*490T>G
NM_000402.4:c.*490T>G	NP_000393.4:n.*490T>G
NM_001042351.2:c.*490T>G	NP_001035810.1:n.*490T>G
XM_005274657.2:c.*490T>G	XP_005274714.1:n.*490T>G
XM_005274658.2:c.*490T>G	XP_005274715.1:n.*490T>G
NM_001360016.2:c.*490T>G MANE Select	NP_001346945.1:n.*490T>G
NM_001042351.3:c.*490T>G	NP_001035810.1:n.*490T>G