Canonical Allele Identifier: CA415232024

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153760275C>G (hg19) ; chrX:g.154532060C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532060C>G , CM000685.2:g.154532060C>G	GRCh38
NC_000023.10:g.153760275C>G , CM000685.1:g.153760275C>G	GRCh37
NC_000023.9:g.153413469C>G	NCBI36
NG_009015.2:g.20513G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1488G>C	ENSP00000377194.2:p.Met496Ile
ENST00000439227.6:c.1491G>C	ENSP00000395599.2:p.Met497Ile
ENST00000696420.1:c.1457+128G>C	ENSP00000512615.1:n.1457+128G>C
ENST00000696421.1:c.1457+128G>C	ENSP00000512616.1:n.1457+128G>C
ENST00000696422.1:c.1351G>C
ENST00000696423.1:c.1354G>C
ENST00000696424.1:c.1340G>C	ENSP00000512619.1:n.1340G>C
ENST00000696425.1:c.*401G>C	ENSP00000512620.1:n.*401G>C
ENST00000696426.1:c.*948G>C	ENSP00000512621.1:n.*948G>C
ENST00000696427.1:c.*448G>C	ENSP00000512622.1:n.*448G>C
ENST00000696428.1:c.*1330G>C	ENSP00000512623.1:n.*1330G>C
ENST00000696429.1:c.1488G>C	ENSP00000512624.1:p.Met496Ile
ENST00000696430.1:c.1488G>C	ENSP00000512625.1:p.Met496Ile
ENST00000393562.10:c.1488G>C MANE Select	ENSP00000377192.3:p.Met496Ile
ENST00000369620.6:c.1626G>C	ENSP00000358633.2:p.Met542Ile
ENST00000393562.6:c.1578G>C	ENSP00000377192.2:p.Met526Ile
ENST00000393564.6:c.1488G>C	ENSP00000377194.2:p.Met496Ile
ENST00000621232.4:c.1488G>C	ENSP00000483686.1:p.Met496Ile
NM_000402.4:c.1578G>C	NP_000393.4:p.Met526Ile
NM_001042351.2:c.1488G>C	NP_001035810.1:p.Met496Ile
XM_005274657.2:c.1581G>C	XP_005274714.1:p.Met527Ile
XM_005274658.2:c.1491G>C	XP_005274715.1:p.Met497Ile
NM_001360016.2:c.1488G>C MANE Select	NP_001346945.1:p.Met496Ile
NM_001042351.3:c.1488G>C	NP_001035810.1:p.Met496Ile