Canonical Allele Identifier: CA337315355
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 1722702
ClinVar RCV Id: RCV002305812
dbSNP Id: rs1050757
MyVariant Identifiers: chrX:g.154531643C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154531643C>T , CM000685.2:g.154531643C>T GRCh38
NG_009015.2:g.20930G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393564.7:c.*357G>A ENSP00000377194.2:n.*357G>A
ENST00000439227.6:c.*357G>A ENSP00000395599.2:n.*357G>A
ENST00000696420.1:c.1457+545G>A ENSP00000512615.1:n.1457+545G>A
ENST00000696421.1:c.1457+545G>A ENSP00000512616.1:n.1457+545G>A
ENST00000696422.1:c.1768G>A
ENST00000696423.1:c.1771G>A
ENST00000696424.1:c.1757G>A ENSP00000512619.1:n.1757G>A
ENST00000696425.1:c.*818G>A ENSP00000512620.1:n.*818G>A
ENST00000696426.1:c.*1365G>A ENSP00000512621.1:n.*1365G>A
ENST00000696427.1:c.*865G>A ENSP00000512622.1:n.*865G>A
ENST00000696428.1:c.*1747G>A ENSP00000512623.1:n.*1747G>A
ENST00000696429.1:c.*357G>A ENSP00000512624.1:n.*357G>A
ENST00000696430.1:c.*357G>A ENSP00000512625.1:n.*357G>A
ENST00000393562.10:c.*357G>A MANE Select ENSP00000377192.3:n.*357G>A
ENST00000393562.6:c.*357G>A ENSP00000377192.2:n.*357G>A
ENST00000621232.4:c.*357G>A ENSP00000483686.1:n.*357G>A
NM_000402.4:c.*357G>A NP_000393.4:n.*357G>A
NM_001042351.2:c.*357G>A NP_001035810.1:n.*357G>A
XM_005274657.2:c.*357G>A XP_005274714.1:n.*357G>A
XM_005274658.2:c.*357G>A XP_005274715.1:n.*357G>A
NM_001360016.2:c.*357G>A MANE Select NP_001346945.1:n.*357G>A
NM_001042351.3:c.*357G>A NP_001035810.1:n.*357G>A