Canonical Allele Identifier: CA415234136

Gene: G6PD

Linked Data

• ClinVar Variation Id: 1722615
• ClinVar RCV Id: RCV002305725
• MyVariant Identifiers: chrX:g.153760928A>G (hg19) ; chrX:g.154532713A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532713A>G , CM000685.2:g.154532713A>G	GRCh38
NC_000023.10:g.153760928A>G , CM000685.1:g.153760928A>G	GRCh37
NC_000023.9:g.153414122A>G	NCBI36
NG_009015.2:g.19860T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.1141T>C	ENSP00000377194.2:p.Phe381Leu
ENST00000439227.6:c.1144T>C	ENSP00000395599.2:p.Phe382Leu
ENST00000696420.1:c.1141T>C	ENSP00000512615.1:p.Phe381Leu
ENST00000696421.1:c.1141T>C	ENSP00000512616.1:p.Phe381Leu
ENST00000696422.1:c.1004T>C
ENST00000696423.1:c.1007T>C
ENST00000696424.1:c.993T>C	ENSP00000512619.1:n.993T>C
ENST00000696425.1:c.*54T>C	ENSP00000512620.1:n.*54T>C
ENST00000696426.1:c.*601T>C	ENSP00000512621.1:n.*601T>C
ENST00000696427.1:c.*101T>C	ENSP00000512622.1:n.*101T>C
ENST00000696428.1:c.*983T>C	ENSP00000512623.1:n.*983T>C
ENST00000696429.1:c.1141T>C	ENSP00000512624.1:p.Phe381Leu
ENST00000696430.1:c.1141T>C	ENSP00000512625.1:p.Phe381Leu
ENST00000393562.10:c.1141T>C MANE Select	ENSP00000377192.3:p.Phe381Leu
ENST00000369620.6:c.1279T>C	ENSP00000358633.2:p.Phe427Leu
ENST00000393562.6:c.1231T>C	ENSP00000377192.2:p.Phe411Leu
ENST00000393564.6:c.1141T>C	ENSP00000377194.2:p.Phe381Leu
ENST00000490651.1:n.362T>C
ENST00000621232.4:c.1141T>C	ENSP00000483686.1:p.Phe381Leu
NM_000402.4:c.1231T>C	NP_000393.4:p.Phe411Leu
NM_001042351.2:c.1141T>C	NP_001035810.1:p.Phe381Leu
XM_005274657.2:c.1234T>C	XP_005274714.1:p.Phe412Leu
XM_005274658.2:c.1144T>C	XP_005274715.1:p.Phe382Leu
XM_011531132.1:c.*54T>C	XP_011529434.1:n.*54T>C
NM_001360016.2:c.1141T>C MANE Select	NP_001346945.1:p.Phe381Leu
NM_001042351.3:c.1141T>C	NP_001035810.1:p.Phe381Leu