Canonical Allele Identifier: CA415234267

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760988C>G (hg19) ; chrX:g.154532773C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532773C>G , CM000685.2:g.154532773C>G	GRCh38
NC_000023.10:g.153760988C>G , CM000685.1:g.153760988C>G	GRCh37
NC_000023.9:g.153414182C>G	NCBI36
NG_009015.2:g.19800G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1081G>C	ENSP00000377194.2:p.Ala361Pro
ENST00000439227.6:c.1084G>C	ENSP00000395599.2:p.Ala362Pro
ENST00000696420.1:c.1081G>C	ENSP00000512615.1:p.Ala361Pro
ENST00000696421.1:c.1081G>C	ENSP00000512616.1:p.Ala361Pro
ENST00000696422.1:c.944G>C
ENST00000696423.1:c.947G>C
ENST00000696424.1:c.933G>C	ENSP00000512619.1:n.933G>C
ENST00000696425.1:c.894G>C	ENSP00000512620.1:p.Arg298Ser
ENST00000696426.1:c.*541G>C	ENSP00000512621.1:n.*541G>C
ENST00000696427.1:c.*41G>C	ENSP00000512622.1:n.*41G>C
ENST00000696428.1:c.*923G>C	ENSP00000512623.1:n.*923G>C
ENST00000696429.1:c.1081G>C	ENSP00000512624.1:p.Ala361Pro
ENST00000696430.1:c.1081G>C	ENSP00000512625.1:p.Ala361Pro
ENST00000393562.10:c.1081G>C MANE Select	ENSP00000377192.3:p.Ala361Pro
ENST00000369620.6:c.1219G>C	ENSP00000358633.2:p.Ala407Pro
ENST00000393562.6:c.1171G>C	ENSP00000377192.2:p.Ala391Pro
ENST00000393564.6:c.1081G>C	ENSP00000377194.2:p.Ala361Pro
ENST00000490651.1:n.302G>C
ENST00000621232.4:c.1081G>C	ENSP00000483686.1:p.Ala361Pro
NM_000402.4:c.1171G>C	NP_000393.4:p.Ala391Pro
NM_001042351.2:c.1081G>C	NP_001035810.1:p.Ala361Pro
XM_005274657.2:c.1174G>C	XP_005274714.1:p.Ala392Pro
XM_005274658.2:c.1084G>C	XP_005274715.1:p.Ala362Pro
XM_011531132.1:c.987G>C	XP_011529434.1:p.Arg329Ser
NM_001360016.2:c.1081G>C MANE Select	NP_001346945.1:p.Ala361Pro
NM_001042351.3:c.1081G>C	NP_001035810.1:p.Ala361Pro