Canonical Allele Identifier: CA2695140396

Gene: G6PD

Linked Data

• gnomAD v4: X-154531647-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531647C>T , CM000685.2:g.154531647C>T	GRCh38
NC_000023.10:g.153759862C>T , CM000685.1:g.153759862C>T	GRCh37
NC_000023.9:g.153413056C>T	NCBI36
NG_009015.2:g.20926G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.*353G>A	ENSP00000377194.2:n.*353G>A
ENST00000439227.6:c.*353G>A	ENSP00000395599.2:n.*353G>A
ENST00000696420.1:c.1457+541G>A	ENSP00000512615.1:n.1457+541G>A
ENST00000696421.1:c.1457+541G>A	ENSP00000512616.1:n.1457+541G>A
ENST00000696422.1:c.1764G>A
ENST00000696423.1:c.1767G>A
ENST00000696424.1:c.1753G>A	ENSP00000512619.1:n.1753G>A
ENST00000696425.1:c.*814G>A	ENSP00000512620.1:n.*814G>A
ENST00000696426.1:c.*1361G>A	ENSP00000512621.1:n.*1361G>A
ENST00000696427.1:c.*861G>A	ENSP00000512622.1:n.*861G>A
ENST00000696428.1:c.*1743G>A	ENSP00000512623.1:n.*1743G>A
ENST00000696429.1:c.*353G>A	ENSP00000512624.1:n.*353G>A
ENST00000696430.1:c.*353G>A	ENSP00000512625.1:n.*353G>A
ENST00000393562.10:c.*353G>A MANE Select	ENSP00000377192.3:n.*353G>A
ENST00000393562.6:c.*353G>A	ENSP00000377192.2:n.*353G>A
ENST00000621232.4:c.*353G>A	ENSP00000483686.1:n.*353G>A
NM_000402.4:c.*353G>A	NP_000393.4:n.*353G>A
NM_001042351.2:c.*353G>A	NP_001035810.1:n.*353G>A
XM_005274657.2:c.*353G>A	XP_005274714.1:n.*353G>A
XM_005274658.2:c.*353G>A	XP_005274715.1:n.*353G>A
NM_001360016.2:c.*353G>A MANE Select	NP_001346945.1:n.*353G>A
NM_001042351.3:c.*353G>A	NP_001035810.1:n.*353G>A