Canonical Allele Identifier:
CA2844606328
Community Standard Title: NM_002121.6(HLA-DPB1):c.[109C>G;111T>G;113T>A;118G>T;119G>T;191T>A;338G>A;341G>A;343C>G;346A>G;374G>A;381T>C;406T>C;441G>A;588T>C;596C>T;624T>C] (p.[Leu37_Phe38delinsGlyTyr;Gly40Leu;Phe64Tyr;Gly113_Met116delinsAspGluAlaVal;Arg125Lys;Thr199Ile])
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.[33080680C>G;33080682T>G;33080684T>A;33080689G>T;33080690G>T;33080762T>A;33080909G>A;33080912G>A;33080914C>G;33080917A>G;33084959G>A;33084966T>C;33084991T>C;33085026G>A;33085173T>C;33085181C>T;33085209T>C] , CM000668.2:g.[33080680C>G;33080682T>G;33080684T>A;33080689G>T;33080690G>T;33080762T>A;33080909G>A;33080912G>A;33080914C>G;33080917A>G;33084959G>A;33084966T>C;33084991T>C;33085026G>A;33085173T>C;33085181C>T;33085209T>C] | GRCh38 |
| NC_000006.11:g.[33048457C>G;33048459T>G;33048461T>A;33048466G>T;33048467G>T;33048539T>A;33048686G>A;33048689G>A;33048691C>G;33048694A>G;33052736G>A;33052743T>C;33052768T>C;33052803G>A;33052950T>C;33052958C>T;33052986T>C] , CM000668.1:g.[33048457C>G;33048459T>G;33048461T>A;33048466G>T;33048467G>T;33048539T>A;33048686G>A;33048689G>A;33048691C>G;33048694A>G;33052736G>A;33052743T>C;33052768T>C;33052803G>A;33052950T>C;33052958C>T;33052986T>C] | GRCh37 |
| NC_000006.10:g.[33156435C>G;33156437T>G;33156439T>A;33156444G>T;33156445G>T;33156517T>A;33156664G>A;33156667G>A;33156669C>G;33156672A>G;33160714G>A;33160721T>C;33160746T>C;33160781G>A;33160928T>C;33160936C>T;33160964T>C] | NCBI36 |
| NG_033241.1:g.[570A>G;598G>A;606A>G;753C>T;788A>G;813A>G;820C>T;4862T>C;4865G>C;4867C>T;4870C>T;5017A>T;5089C>A;5090C>A;5095A>T;5097A>C;5099G>C] | |
| NG_033242.1:g.[9755C>G;9757T>G;9759T>A;9764G>T;9765G>T;9837T>A;9984G>A;9987G>A;9989C>G;9992A>G;14034G>A;14041T>C;14066T>C;14101G>A;14248T>C;14256C>T;14284T>C] |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002121.6:c.[109C>G;111T>G;113T>A;118G>T;119G>T;191T>A;338G>A;341G>A;343C>G;346A>G;374G>A;381T>C;406T>C;441G>A;588T>C;596C>T;624T>C] MANE Select | NP_002112.3:p.[Leu37Gly;Phe38Tyr;Gly40Leu;Phe64Tyr;Gly113Asp;... |
| ENST00000418931.7:c.[109C>G;111T>G;113T>A;118G>T;119G>T;191T>A;338G>A;341G>A;343C>G;346A>G;374G>A;381T>C;406T>C;441G>A;588T>C;596C>T;624T>C] MANE Select | ENSP00000408146.2:p.[Leu37Gly;Phe38Tyr;Gly40Leu;Phe64Tyr;Gly1... |
| NM_002121.5:c.[109C>G;111T>G;113T>A;118G>T;119G>T;191T>A;338G>A;341G>A;343C>G;346A>G;374G>A;381T>C;406T>C;441G>A;588T>C;596C>T;624T>C] | NP_002112.3:p.[Leu37Val;Phe38Asn;Gly40Leu;Phe64Tyr;Gly113Asp;... |
| ENST00000416804.1:c.[9C>G;11T>G;13T>A;18G>T;19G>T;91T>A;238G>A;241G>A;243C>G;246A>G;274G>A;281T>C;306T>C;341G>A;488T>C;496C>T;524T>C] | |
| ENST00000418931.6:c.[109C>G;111T>G;113T>A;118G>T;119G>T;191T>A;338G>A;341G>A;343C>G;346A>G;374G>A;381T>C;406T>C;441G>A;588T>C;596C>T;624T>C] | ENSP00000408146.2:p.[Leu37Val;Phe38Asn;Gly40Leu;Phe64Tyr;Gly1... |
| ENST00000428835.5:c.[49-9C>G;49-7T>G;49-5T>A;49G>T;50G>T;122T>A;269G>A;272G>A;274C>G;277A>G;305G>A;312T>C;337T>C;372G>A;519T>C;527C>T;555T>C] | ENSP00000412654.1:p.Gly17Ter |
| ENST00000498038.1:n.[238C>G;240T>G;242T>A;247G>T;248G>T;320T>A;467G>A;470G>A;472C>G;475A>G;503G>A;510T>C;535T>C;570G>A;717T>C;725C>T;753T>C] | |
| XM_006715078.2:c.[-204C>G;-202T>G;-200T>A;-195G>T;-194G>T;-122T>A;26G>A;29G>A;31C>G;34A>G;62G>A;69T>C;94T>C;129G>A;276T>C;284C>T;312T>C] | XP_006715141.1:p.[Gly9Asp;Gly10_Pro11delinsGluAla;Met12Val;Ar... |