Canonical Allele Identifier: CA873344005
Gene: G6PD HGNC NCBI

Linked Data

dbSNP Id: rs1239029899
MyVariant Identifiers: chrX:g.154534298C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154534298C>T , CM000685.2:g.154534298C>T GRCh38
NC_000023.10:g.153762513C>T , CM000685.1:g.153762513C>T GRCh37
NC_000023.9:g.153415707C>T NCBI36
NG_009015.2:g.18275G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393564.7:c.644+40G>A ENSP00000377194.2:n.644+40G>A
ENST00000439227.6:c.647+40G>A ENSP00000395599.2:n.647+40G>A
ENST00000696420.1:c.644+40G>A ENSP00000512615.1:n.644+40G>A
ENST00000696421.1:c.644+40G>A ENSP00000512616.1:n.644+40G>A
ENST00000696422.1:c.507+40G>A
ENST00000696423.1:c.510+40G>A
ENST00000696424.1:c.524+40G>A ENSP00000512619.1:n.524+40G>A
ENST00000696425.1:c.644+40G>A ENSP00000512620.1:n.644+40G>A
ENST00000696426.1:c.644+40G>A ENSP00000512621.1:n.644+40G>A
ENST00000696427.1:c.644+40G>A ENSP00000512622.1:n.644+40G>A
ENST00000696428.1:c.*486+40G>A ENSP00000512623.1:n.*486+40G>A
ENST00000696429.1:c.644+40G>A ENSP00000512624.1:n.644+40G>A
ENST00000696430.1:c.644+40G>A ENSP00000512625.1:n.644+40G>A
ENST00000393562.10:c.644+40G>A MANE Select ENSP00000377192.3:n.644+40G>A
ENST00000369620.6:c.644+40G>A ENSP00000358633.2:n.644+40G>A
ENST00000393562.6:c.734+40G>A ENSP00000377192.2:n.734+40G>A
ENST00000393564.6:c.644+40G>A ENSP00000377194.2:n.644+40G>A
ENST00000433845.1:c.644+40G>A ENSP00000394690.1:n.644+40G>A
ENST00000439227.5:c.647+40G>A ENSP00000395599.1:n.647+40G>A
ENST00000440967.5:c.647+40G>A ENSP00000400648.1:n.647+40G>A
ENST00000621232.4:c.644+40G>A ENSP00000483686.1:n.644+40G>A
NM_000402.4:c.734+40G>A NP_000393.4:n.734+40G>A
NM_001042351.2:c.644+40G>A NP_001035810.1:n.644+40G>A
XM_005274657.2:c.737+40G>A XP_005274714.1:n.737+40G>A
XM_005274658.2:c.647+40G>A XP_005274715.1:n.647+40G>A
XM_011531132.1:c.737+40G>A XP_011529434.1:n.737+40G>A
NM_001360016.2:c.644+40G>A MANE Select NP_001346945.1:n.644+40G>A
NM_001042351.3:c.644+40G>A NP_001035810.1:n.644+40G>A