Canonical Allele Identifier: CA1281319699
Gene: DPP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.115768324G= , CM000664.2:g.115768324G= GRCh38
NC_000002.11:g.116525900G= , CM000664.1:g.116525900G= GRCh37
NC_000002.10:g.116242370G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410059.6:c.1141G= MANE Select ENSP00000386565.1:p.Gly381=
ENST00000310323.12:c.1120G= ENSP00000309066.8:p.Gly374=
ENST00000393147.6:c.1153G= ENSP00000376855.2:p.Gly385=
ENST00000409163.5:c.991G= ENSP00000387038.1:p.Gly331=
ENST00000410059.5:c.1141G= ENSP00000386565.1:p.Gly381=
NM_001004360.3:c.1120G= NP_001004360.2:p.Gly374=
NM_001178034.1:c.1153G= NP_001171505.1:p.Gly385=
NM_001178036.1:c.991G= NP_001171507.1:p.Gly331=
NM_001178037.1:c.1129G= NP_001171508.1:p.Gly377=
NM_020868.3:c.1141G= NP_065919.2:p.Gly381=
XM_011511526.1:c.1120G= XP_011509828.1:p.Gly374=
XM_011511527.1:c.991G= XP_011509829.1:p.Gly331=
XM_011511528.1:c.889G= XP_011509830.1:p.Gly297=
NM_001321905.1:c.1192G= NP_001308834.1:p.Gly398=
NM_001321906.1:c.1120G= NP_001308835.1:p.Gly374=
NM_001321907.1:c.1102G= NP_001308836.1:p.Gly368=
NM_001321908.1:c.1051G= NP_001308837.1:p.Gly351=
NM_001321909.1:c.1024G= NP_001308838.1:p.Gly342=
NM_001321910.1:c.991G= NP_001308839.1:p.Gly331=
NM_001321911.1:c.991G= NP_001308840.1:p.Gly331=
NM_001321912.1:c.991G= NP_001308841.1:p.Gly331=
NM_001321913.1:c.379G= NP_001308842.1:p.Gly127=
NM_001321914.1:c.379G= NP_001308843.1:p.Gly127=
NM_020868.4:c.1141G= NP_065919.2:p.Gly381=
XM_017004566.1:c.1018G= XP_016860055.1:p.Gly340=
XM_024453023.1:c.1081G= XP_024308791.1:p.Gly361=
NM_001004360.4:c.1120G= NP_001004360.3:p.Gly374=
NM_001178036.2:c.991G= NP_001171507.2:p.Gly331=
NM_001178037.2:c.1129G= NP_001171508.2:p.Gly377=
NM_001321905.2:c.1192G= NP_001308834.2:p.Gly398=
NM_001321907.2:c.1102G= NP_001308836.2:p.Gly368=
NM_001321908.2:c.1051G= NP_001308837.2:p.Gly351=
NM_001321909.2:c.1024G= NP_001308838.2:p.Gly342=
NM_001321910.2:c.991G= NP_001308839.2:p.Gly331=
NM_001321911.2:c.991G= NP_001308840.2:p.Gly331=
NM_001321912.2:c.991G= NP_001308841.2:p.Gly331=
NM_001321913.2:c.379G= NP_001308842.2:p.Gly127=
NM_020868.6:c.1141G= MANE Select NP_065919.3:p.Gly381=
NM_001004360.5:c.1120G= NP_001004360.3:p.Gly374=
NM_001178036.3:c.991G= NP_001171507.2:p.Gly331=
NM_001178037.3:c.1129G= NP_001171508.2:p.Gly377=
NM_001321905.3:c.1192G= NP_001308834.2:p.Gly398=
NM_001321906.2:c.1120G= NP_001308835.2:p.Gly374=
NM_001321907.3:c.1102G= NP_001308836.2:p.Gly368=
NM_001321908.3:c.1051G= NP_001308837.2:p.Gly351=
NM_001321909.3:c.1024G= NP_001308838.2:p.Gly342=
NM_001321910.3:c.991G= NP_001308839.2:p.Gly331=
NM_001321911.3:c.991G= NP_001308840.2:p.Gly331=
NM_001321912.3:c.991G= NP_001308841.2:p.Gly331=
NM_001321913.3:c.379G= NP_001308842.2:p.Gly127=
NM_001321914.2:c.379G= NP_001308843.2:p.Gly127=
NM_001399849.1:c.991G= NP_001386778.1:p.Gly331=
NM_001399850.1:c.379G= NP_001386779.1:p.Gly127=
NM_001399851.1:c.889G= NP_001386780.1:p.Gly297=