Canonical Allele Identifier: CA415237832

Gene: G6PD

Linked Data

• MyVariant Identifiers: chrX:g.153762600G>C (hg19) ; chrX:g.154534385G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154534385G>C , CM000685.2:g.154534385G>C	GRCh38
NC_000023.10:g.153762600G>C , CM000685.1:g.153762600G>C	GRCh37
NC_000023.9:g.153415794G>C	NCBI36
NG_009015.2:g.18188C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.597C>G	ENSP00000377194.2:p.Ile199Met
ENST00000439227.6:c.600C>G	ENSP00000395599.2:p.Ile200Met
ENST00000696420.1:c.597C>G	ENSP00000512615.1:p.Ile199Met
ENST00000696421.1:c.597C>G	ENSP00000512616.1:p.Ile199Met
ENST00000696422.1:c.460C>G
ENST00000696423.1:c.463C>G
ENST00000696424.1:c.477C>G	ENSP00000512619.1:p.Ile159Met
ENST00000696425.1:c.597C>G	ENSP00000512620.1:p.Ile199Met
ENST00000696426.1:c.597C>G	ENSP00000512621.1:p.Ile199Met
ENST00000696427.1:c.597C>G	ENSP00000512622.1:p.Ile199Met
ENST00000696428.1:c.*439C>G	ENSP00000512623.1:n.*439C>G
ENST00000696429.1:c.597C>G	ENSP00000512624.1:p.Ile199Met
ENST00000696430.1:c.597C>G	ENSP00000512625.1:p.Ile199Met
ENST00000393562.10:c.597C>G MANE Select	ENSP00000377192.3:p.Ile199Met
ENST00000369620.6:c.597C>G	ENSP00000358633.2:p.Ile199Met
ENST00000393562.6:c.687C>G	ENSP00000377192.2:p.Ile229Met
ENST00000393564.6:c.597C>G	ENSP00000377194.2:p.Ile199Met
ENST00000433845.1:c.597C>G	ENSP00000394690.1:p.Ile199Met
ENST00000439227.5:c.600C>G	ENSP00000395599.1:p.Ile200Met
ENST00000440967.5:c.600C>G	ENSP00000400648.1:p.Ile200Met
ENST00000621232.4:c.597C>G	ENSP00000483686.1:p.Ile199Met
NM_000402.4:c.687C>G	NP_000393.4:p.Ile229Met
NM_001042351.2:c.597C>G	NP_001035810.1:p.Ile199Met
XM_005274657.2:c.690C>G	XP_005274714.1:p.Ile230Met
XM_005274658.2:c.600C>G	XP_005274715.1:p.Ile200Met
XM_011531132.1:c.690C>G	XP_011529434.1:p.Ile230Met
NM_001360016.2:c.597C>G MANE Select	NP_001346945.1:p.Ile199Met
NM_001042351.3:c.597C>G	NP_001035810.1:p.Ile199Met