Canonical Allele Identifier: CA645178418

Gene: G6PD

Linked Data

• dbSNP Id: rs1569556168
• gnomAD v2: X-153759695-CGGGTGGCACG-C
• gnomAD v3: X-154531480-CGGGTGGCACG-C
• gnomAD v4: X-154531480-CGGGTGGCACG-C
• MyVariant Identifiers: chrX:g.153759696_153759705del (hg19) ; chrX:g.154531481_154531490del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154531488_154531497del , CM000685.2:g.154531488_154531497del	GRCh38
NC_000023.10:g.153759703_153759712del , CM000685.1:g.153759703_153759712del	GRCh37
NC_000023.9:g.153412897_153412906del	NCBI36
NG_009015.2:g.21083_21092del

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.*510_*519del	ENSP00000377194.2:n.*510_*519del
ENST00000439227.6:c.*510_*519del	ENSP00000395599.2:n.*510_*519del
ENST00000696420.1:c.1457+698_1457+707del	ENSP00000512615.1:n.1457+698_1457+707del
ENST00000696421.1:c.1457+698_1457+707del	ENSP00000512616.1:n.1457+698_1457+707del
ENST00000696422.1:c.1921_1930del
ENST00000696423.1:c.1924_1933del
ENST00000696424.1:c.1910_1919del	ENSP00000512619.1:n.1910_1919del
ENST00000696425.1:c.*971_*980del	ENSP00000512620.1:n.*971_*980del
ENST00000696426.1:c.*1518_*1527del	ENSP00000512621.1:n.*1518_*1527del
ENST00000696427.1:c.*1018_*1027del	ENSP00000512622.1:n.*1018_*1027del
ENST00000696428.1:c.*1900_*1909del	ENSP00000512623.1:n.*1900_*1909del
ENST00000696429.1:c.*510_*519del	ENSP00000512624.1:n.*510_*519del
ENST00000696430.1:c.*510_*519del	ENSP00000512625.1:n.*510_*519del
ENST00000393562.10:c.*510_*519del MANE Select	ENSP00000377192.3:n.*510_*519del
ENST00000393562.6:c.*510_*519del	ENSP00000377192.2:n.*510_*519del
ENST00000621232.4:c.*510_*519del	ENSP00000483686.1:n.*510_*519del
NM_000402.4:c.*510_*519del	NP_000393.4:n.*510_*519del
NM_001042351.2:c.*510_*519del	NP_001035810.1:n.*510_*519del
XM_005274657.2:c.*510_*519del	XP_005274714.1:n.*510_*519del
XM_005274658.2:c.*510_*519del	XP_005274715.1:n.*510_*519del
NM_001360016.2:c.*510_*519del MANE Select	NP_001346945.1:n.*510_*519del
NM_001042351.3:c.*510_*519del	NP_001035810.1:n.*510_*519del