Canonical Allele Identifier: CA2580573390

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.[154532695G>A;154535277T>C] , CM000685.2:g.[154532695G>A;154535277T>C]	GRCh38
NC_000023.10:g.[153760910G>A;153763492T>C] , CM000685.1:g.[153760910G>A;153763492T>C]	GRCh37
NC_000023.9:g.[153414104G>A;153416686T>C]	NCBI36
NG_009015.2:g.[17296A>G;19878C>T]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.[376A>G;1159C>T]	ENSP00000377194.2:p.[Asn126Asp;Arg387Cys]
ENST00000439227.6:c.[376A>G;1162C>T]	ENSP00000395599.2:p.[Asn126Asp;Arg388Cys]
ENST00000696420.1:c.[376A>G;1159C>T]	ENSP00000512615.1:p.[Asn126Asp;Arg387Cys]
ENST00000696421.1:c.[376A>G;1159C>T]	ENSP00000512616.1:p.[Asn126Asp;Arg387Cys]
ENST00000696422.1:c.[239A>G;1022C>T]
ENST00000696423.1:c.[239A>G;1025C>T]
ENST00000696424.1:c.[256A>G;1011C>T]	ENSP00000512619.1:[p.Asn86Asp;n.1011C>T]
ENST00000696425.1:c.[376A>G;*72C>T]	ENSP00000512620.1:[p.Asn126Asp;n.*72C>T]
ENST00000696426.1:c.[376A>G;*619C>T]	ENSP00000512621.1:[p.Asn126Asp;n.*619C>T]
ENST00000696427.1:c.[376A>G;*119C>T]	ENSP00000512622.1:[p.Asn126Asp;n.*119C>T]
ENST00000696428.1:c.[*218A>G;*1001C>T]	ENSP00000512623.1:n.[*218A>G;*1001C>T]
ENST00000696429.1:c.[376A>G;1159C>T]	ENSP00000512624.1:p.[Asn126Asp;Arg387Cys]
ENST00000696430.1:c.[376A>G;1159C>T]	ENSP00000512625.1:p.[Asn126Asp;Arg387Cys]
ENST00000393562.10:c.[376A>G;1159C>T] MANE Select	ENSP00000377192.3:p.[Asn126Asp;Arg387Cys]
ENST00000369620.6:c.[376A>G;1297C>T]	ENSP00000358633.2:p.[Asn126Asp;Arg433Cys]
ENST00000393562.6:c.[466A>G;1249C>T]	ENSP00000377192.2:p.[Asn156Asp;Arg417Cys]
ENST00000393564.6:c.[376A>G;1159C>T]	ENSP00000377194.2:p.[Asn126Asp;Arg387Cys]
ENST00000621232.4:c.[376A>G;1159C>T]	ENSP00000483686.1:p.[Asn126Asp;Arg387Cys]
NM_000402.4:c.[466A>G;1249C>T]	NP_000393.4:p.[Asn156Asp;Arg417Cys]
NM_001042351.2:c.[376A>G;1159C>T]	NP_001035810.1:p.[Asn126Asp;Arg387Cys]
XM_005274657.2:c.[466A>G;1252C>T]	XP_005274714.1:p.[Asn156Asp;Arg418Cys]
XM_005274658.2:c.[376A>G;1162C>T]	XP_005274715.1:p.[Asn126Asp;Arg388Cys]
XM_011531132.1:c.[466A>G;*72C>T]	XP_011529434.1:[p.Asn156Asp;n.*72C>T]
NM_001360016.2:c.[376A>G;1159C>T] MANE Select	NP_001346945.1:p.[Asn126Asp;Arg387Cys]
NM_001042351.3:c.[376A>G;1159C>T]	NP_001035810.1:p.[Asn126Asp;Arg387Cys]