Canonical Allele Identifier: CA415234684

Gene: G6PD

Linked Data

• COSMIC: COSM3034519 ; COSM3034520 ; COSM4378406
• MyVariant Identifiers: chrX:g.153761274G>A (hg19) ; chrX:g.154533059G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533059G>A , CM000685.2:g.154533059G>A	GRCh38
NC_000023.10:g.153761274G>A , CM000685.1:g.153761274G>A	GRCh37
NC_000023.9:g.153414468G>A	NCBI36
NG_009015.2:g.19514C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.934C>T	ENSP00000377194.2:p.Pro312Ser
ENST00000439227.6:c.937C>T	ENSP00000395599.2:p.Pro313Ser
ENST00000696420.1:c.934C>T	ENSP00000512615.1:p.Pro312Ser
ENST00000696421.1:c.934C>T	ENSP00000512616.1:p.Pro312Ser
ENST00000696422.1:c.797C>T
ENST00000696423.1:c.800C>T
ENST00000696424.1:c.786C>T	ENSP00000512619.1:n.786C>T
ENST00000696425.1:c.865-257C>T	ENSP00000512620.1:n.865-257C>T
ENST00000696426.1:c.*394C>T	ENSP00000512621.1:n.*394C>T
ENST00000696427.1:c.941C>T	ENSP00000512622.1:p.Pro314Leu
ENST00000696428.1:c.*776C>T	ENSP00000512623.1:n.*776C>T
ENST00000696429.1:c.934C>T	ENSP00000512624.1:p.Pro312Ser
ENST00000696430.1:c.934C>T	ENSP00000512625.1:p.Pro312Ser
ENST00000393562.10:c.934C>T MANE Select	ENSP00000377192.3:p.Pro312Ser
ENST00000369620.6:c.1072C>T	ENSP00000358633.2:p.Pro358Ser
ENST00000393562.6:c.1024C>T	ENSP00000377192.2:p.Pro342Ser
ENST00000393564.6:c.934C>T	ENSP00000377194.2:p.Pro312Ser
ENST00000439227.5:c.937C>T	ENSP00000395599.1:p.Pro313Ser
ENST00000440967.5:c.937C>T	ENSP00000400648.1:p.Pro313Ser
ENST00000490651.1:n.16C>T
ENST00000621232.4:c.934C>T	ENSP00000483686.1:p.Pro312Ser
NM_000402.4:c.1024C>T	NP_000393.4:p.Pro342Ser
NM_001042351.2:c.934C>T	NP_001035810.1:p.Pro312Ser
XM_005274657.2:c.1027C>T	XP_005274714.1:p.Pro343Ser
XM_005274658.2:c.937C>T	XP_005274715.1:p.Pro313Ser
XM_011531132.1:c.958-257C>T	XP_011529434.1:n.958-257C>T
NM_001360016.2:c.934C>T MANE Select	NP_001346945.1:p.Pro312Ser
NM_001042351.3:c.934C>T	NP_001035810.1:p.Pro312Ser