Canonical Allele Identifier: CA10565997

Gene: G6PD

Linked Data

• dbSNP Id: rs782611676
• ExAC: X:153760367 G / A
• gnomAD v2: X-153760367-G-A
• gnomAD v3: X-154532152-G-A
• gnomAD v4: X-154532152-G-A
• MyVariant Identifiers: chrX:g.153760367G>A (hg19) ; chrX:g.154532152G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532152G>A , CM000685.2:g.154532152G>A	GRCh38
NC_000023.10:g.153760367G>A , CM000685.1:g.153760367G>A	GRCh37
NC_000023.9:g.153413561G>A	NCBI36
NG_009015.2:g.20421C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1457+36C>T	ENSP00000377194.2:n.1457+36C>T
ENST00000439227.6:c.1460+36C>T	ENSP00000395599.2:n.1460+36C>T
ENST00000696420.1:c.1457+36C>T	ENSP00000512615.1:n.1457+36C>T
ENST00000696421.1:c.1457+36C>T	ENSP00000512616.1:n.1457+36C>T
ENST00000696422.1:c.1320+36C>T
ENST00000696423.1:c.1323+36C>T
ENST00000696424.1:c.1309+36C>T	ENSP00000512619.1:n.1309+36C>T
ENST00000696425.1:c.*370+36C>T	ENSP00000512620.1:n.*370+36C>T
ENST00000696426.1:c.*917+36C>T	ENSP00000512621.1:n.*917+36C>T
ENST00000696427.1:c.*417+36C>T	ENSP00000512622.1:n.*417+36C>T
ENST00000696428.1:c.*1299+36C>T	ENSP00000512623.1:n.*1299+36C>T
ENST00000696429.1:c.1457+36C>T	ENSP00000512624.1:n.1457+36C>T
ENST00000696430.1:c.1457+36C>T	ENSP00000512625.1:n.1457+36C>T
ENST00000393562.10:c.1457+36C>T MANE Select	ENSP00000377192.3:n.1457+36C>T
ENST00000369620.6:c.1595+36C>T	ENSP00000358633.2:n.1595+36C>T
ENST00000393562.6:c.1547+36C>T	ENSP00000377192.2:n.1547+36C>T
ENST00000393564.6:c.1457+36C>T	ENSP00000377194.2:n.1457+36C>T
ENST00000490651.1:n.714C>T
ENST00000621232.4:c.1457+36C>T	ENSP00000483686.1:n.1457+36C>T
NM_000402.4:c.1547+36C>T	NP_000393.4:n.1547+36C>T
NM_001042351.2:c.1457+36C>T	NP_001035810.1:n.1457+36C>T
XM_005274657.2:c.1550+36C>T	XP_005274714.1:n.1550+36C>T
XM_005274658.2:c.1460+36C>T	XP_005274715.1:n.1460+36C>T
NM_001360016.2:c.1457+36C>T MANE Select	NP_001346945.1:n.1457+36C>T
NM_001042351.3:c.1457+36C>T	NP_001035810.1:n.1457+36C>T