Canonical Allele Identifier: CA10646061

Gene: G6PD

Linked Data

• ClinVar Variation Id: 368093
• ClinVar RCV Id: RCV000270535
• dbSNP Id: rs1057515820
• gnomAD v2: X-153759680-C-A
• gnomAD v3: X-154531465-C-A
• gnomAD v4: X-154531465-C-A
• MyVariant Identifiers: chrX:g.153759680C>A (hg19) ; chrX:g.154531465C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531465C>A , CM000685.2:g.154531465C>A	GRCh38
NC_000023.10:g.153759680C>A , CM000685.1:g.153759680C>A	GRCh37
NC_000023.9:g.153412874C>A	NCBI36
NG_009015.2:g.21108G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.*535G>T	ENSP00000377194.2:n.*535G>T
ENST00000439227.6:c.*535G>T	ENSP00000395599.2:n.*535G>T
ENST00000696420.1:c.1457+723G>T	ENSP00000512615.1:n.1457+723G>T
ENST00000696421.1:c.1457+723G>T	ENSP00000512616.1:n.1457+723G>T
ENST00000696422.1:c.1946G>T
ENST00000696423.1:c.1949G>T
ENST00000696424.1:c.1935G>T	ENSP00000512619.1:n.1935G>T
ENST00000696425.1:c.*996G>T	ENSP00000512620.1:n.*996G>T
ENST00000696426.1:c.*1543G>T	ENSP00000512621.1:n.*1543G>T
ENST00000696427.1:c.*1043G>T	ENSP00000512622.1:n.*1043G>T
ENST00000696428.1:c.*1925G>T	ENSP00000512623.1:n.*1925G>T
ENST00000696429.1:c.*535G>T	ENSP00000512624.1:n.*535G>T
ENST00000696430.1:c.*535G>T	ENSP00000512625.1:n.*535G>T
ENST00000393562.10:c.*535G>T MANE Select	ENSP00000377192.3:n.*535G>T
ENST00000393562.6:c.*535G>T	ENSP00000377192.2:n.*535G>T
ENST00000621232.4:c.*535G>T	ENSP00000483686.1:n.*535G>T
NM_000402.4:c.*535G>T	NP_000393.4:n.*535G>T
NM_001042351.2:c.*535G>T	NP_001035810.1:n.*535G>T
XM_005274657.2:c.*535G>T	XP_005274714.1:n.*535G>T
XM_005274658.2:c.*535G>T	XP_005274715.1:n.*535G>T
NM_001360016.2:c.*535G>T MANE Select	NP_001346945.1:n.*535G>T
NM_001042351.3:c.*535G>T	NP_001035810.1:n.*535G>T