Canonical Allele Identifier: CA415234970

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153761342A>G (hg19) ; chrX:g.154533127A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533127A>G , CM000685.2:g.154533127A>G	GRCh38
NC_000023.10:g.153761342A>G , CM000685.1:g.153761342A>G	GRCh37
NC_000023.9:g.153414536A>G	NCBI36
NG_009015.2:g.19446T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393564.7:c.866T>C	ENSP00000377194.2:p.Val289Ala
ENST00000439227.6:c.869T>C	ENSP00000395599.2:p.Val290Ala
ENST00000696420.1:c.866T>C	ENSP00000512615.1:p.Val289Ala
ENST00000696421.1:c.866T>C	ENSP00000512616.1:p.Val289Ala
ENST00000696422.1:c.729T>C
ENST00000696423.1:c.732T>C
ENST00000696424.1:c.718T>C	ENSP00000512619.1:p.Ser240Pro
ENST00000696425.1:c.865-325T>C	ENSP00000512620.1:n.865-325T>C
ENST00000696426.1:c.*326T>C	ENSP00000512621.1:n.*326T>C
ENST00000696427.1:c.873T>C	ENSP00000512622.1:p.Gly291=
ENST00000696428.1:c.*708T>C	ENSP00000512623.1:n.*708T>C
ENST00000696429.1:c.866T>C	ENSP00000512624.1:p.Val289Ala
ENST00000696430.1:c.866T>C	ENSP00000512625.1:p.Val289Ala
ENST00000393562.10:c.866T>C MANE Select	ENSP00000377192.3:p.Val289Ala
ENST00000369620.6:c.1004T>C	ENSP00000358633.2:p.Val335Ala
ENST00000393562.6:c.956T>C	ENSP00000377192.2:p.Val319Ala
ENST00000393564.6:c.866T>C	ENSP00000377194.2:p.Val289Ala
ENST00000439227.5:c.869T>C	ENSP00000395599.1:p.Val290Ala
ENST00000440967.5:c.869T>C	ENSP00000400648.1:p.Val290Ala
ENST00000621232.4:c.866T>C	ENSP00000483686.1:p.Val289Ala
NM_000402.4:c.956T>C	NP_000393.4:p.Val319Ala
NM_001042351.2:c.866T>C	NP_001035810.1:p.Val289Ala
XM_005274657.2:c.959T>C	XP_005274714.1:p.Val320Ala
XM_005274658.2:c.869T>C	XP_005274715.1:p.Val290Ala
XM_011531132.1:c.958-325T>C	XP_011529434.1:n.958-325T>C
NM_001360016.2:c.866T>C MANE Select	NP_001346945.1:p.Val289Ala
NM_001042351.3:c.866T>C	NP_001035810.1:p.Val289Ala