Canonical Allele Identifier: CA2579741993

Gene: G6PD

Linked Data

• ClinVar Variation Id: 2777199
• ClinVar RCV Id: RCV003621735

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532177C>A , CM000685.2:g.154532177C>A	GRCh38
NC_000023.10:g.153760392C>A , CM000685.1:g.153760392C>A	GRCh37
NC_000023.9:g.153413586C>A	NCBI36
NG_009015.2:g.20396G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1457+11G>T	ENSP00000377194.2:n.1457+11G>T
ENST00000439227.6:c.1460+11G>T	ENSP00000395599.2:n.1460+11G>T
ENST00000696420.1:c.1457+11G>T	ENSP00000512615.1:n.1457+11G>T
ENST00000696421.1:c.1457+11G>T	ENSP00000512616.1:n.1457+11G>T
ENST00000696422.1:c.1320+11G>T
ENST00000696423.1:c.1323+11G>T
ENST00000696424.1:c.1309+11G>T	ENSP00000512619.1:n.1309+11G>T
ENST00000696425.1:c.*370+11G>T	ENSP00000512620.1:n.*370+11G>T
ENST00000696426.1:c.*917+11G>T	ENSP00000512621.1:n.*917+11G>T
ENST00000696427.1:c.*417+11G>T	ENSP00000512622.1:n.*417+11G>T
ENST00000696428.1:c.*1299+11G>T	ENSP00000512623.1:n.*1299+11G>T
ENST00000696429.1:c.1457+11G>T	ENSP00000512624.1:n.1457+11G>T
ENST00000696430.1:c.1457+11G>T	ENSP00000512625.1:n.1457+11G>T
ENST00000393562.10:c.1457+11G>T MANE Select	ENSP00000377192.3:n.1457+11G>T
ENST00000369620.6:c.1595+11G>T	ENSP00000358633.2:n.1595+11G>T
ENST00000393562.6:c.1547+11G>T	ENSP00000377192.2:n.1547+11G>T
ENST00000393564.6:c.1457+11G>T	ENSP00000377194.2:n.1457+11G>T
ENST00000490651.1:n.689G>T
ENST00000621232.4:c.1457+11G>T	ENSP00000483686.1:n.1457+11G>T
NM_000402.4:c.1547+11G>T	NP_000393.4:n.1547+11G>T
NM_001042351.2:c.1457+11G>T	NP_001035810.1:n.1457+11G>T
XM_005274657.2:c.1550+11G>T	XP_005274714.1:n.1550+11G>T
XM_005274658.2:c.1460+11G>T	XP_005274715.1:n.1460+11G>T
NM_001360016.2:c.1457+11G>T MANE Select	NP_001346945.1:n.1457+11G>T
NM_001042351.3:c.1457+11G>T	NP_001035810.1:n.1457+11G>T