Canonical Allele Identifier: CA2695139728

Gene: G6PD

Linked Data

• gnomAD v4: X-154531514-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531514G>T , CM000685.2:g.154531514G>T	GRCh38
NC_000023.10:g.153759729G>T , CM000685.1:g.153759729G>T	GRCh37
NC_000023.9:g.153412923G>T	NCBI36
NG_009015.2:g.21059C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.*486C>A	ENSP00000377194.2:n.*486C>A
ENST00000439227.6:c.*486C>A	ENSP00000395599.2:n.*486C>A
ENST00000696420.1:c.1457+674C>A	ENSP00000512615.1:n.1457+674C>A
ENST00000696421.1:c.1457+674C>A	ENSP00000512616.1:n.1457+674C>A
ENST00000696422.1:c.1897C>A
ENST00000696423.1:c.1900C>A
ENST00000696424.1:c.1886C>A	ENSP00000512619.1:n.1886C>A
ENST00000696425.1:c.*947C>A	ENSP00000512620.1:n.*947C>A
ENST00000696426.1:c.*1494C>A	ENSP00000512621.1:n.*1494C>A
ENST00000696427.1:c.*994C>A	ENSP00000512622.1:n.*994C>A
ENST00000696428.1:c.*1876C>A	ENSP00000512623.1:n.*1876C>A
ENST00000696429.1:c.*486C>A	ENSP00000512624.1:n.*486C>A
ENST00000696430.1:c.*486C>A	ENSP00000512625.1:n.*486C>A
ENST00000393562.10:c.*486C>A MANE Select	ENSP00000377192.3:n.*486C>A
ENST00000393562.6:c.*486C>A	ENSP00000377192.2:n.*486C>A
ENST00000621232.4:c.*486C>A	ENSP00000483686.1:n.*486C>A
NM_000402.4:c.*486C>A	NP_000393.4:n.*486C>A
NM_001042351.2:c.*486C>A	NP_001035810.1:n.*486C>A
XM_005274657.2:c.*486C>A	XP_005274714.1:n.*486C>A
XM_005274658.2:c.*486C>A	XP_005274715.1:n.*486C>A
NM_001360016.2:c.*486C>A MANE Select	NP_001346945.1:n.*486C>A
NM_001042351.3:c.*486C>A	NP_001035810.1:n.*486C>A