Canonical Allele Identifier: CA348324413
Gene: DPP10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.115768333T>A , CM000664.2:g.115768333T>A GRCh38
NC_000002.11:g.116525909T>A , CM000664.1:g.116525909T>A GRCh37
NC_000002.10:g.116242379T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410059.6:c.1150T>A MANE Select ENSP00000386565.1:p.Phe384Ile
ENST00000310323.12:c.1129T>A ENSP00000309066.8:p.Phe377Ile
ENST00000393147.6:c.1162T>A ENSP00000376855.2:p.Phe388Ile
ENST00000409163.5:c.1000T>A ENSP00000387038.1:p.Phe334Ile
ENST00000410059.5:c.1150T>A ENSP00000386565.1:p.Phe384Ile
NM_001004360.3:c.1129T>A NP_001004360.2:p.Phe377Ile
NM_001178034.1:c.1162T>A NP_001171505.1:p.Phe388Ile
NM_001178036.1:c.1000T>A NP_001171507.1:p.Phe334Ile
NM_001178037.1:c.1138T>A NP_001171508.1:p.Phe380Ile
NM_020868.3:c.1150T>A NP_065919.2:p.Phe384Ile
XM_011511526.1:c.1129T>A XP_011509828.1:p.Phe377Ile
XM_011511527.1:c.1000T>A XP_011509829.1:p.Phe334Ile
XM_011511528.1:c.898T>A XP_011509830.1:p.Phe300Ile
NM_001321905.1:c.1201T>A NP_001308834.1:p.Phe401Ile
NM_001321906.1:c.1129T>A NP_001308835.1:p.Phe377Ile
NM_001321907.1:c.1111T>A NP_001308836.1:p.Phe371Ile
NM_001321908.1:c.1060T>A NP_001308837.1:p.Phe354Ile
NM_001321909.1:c.1033T>A NP_001308838.1:p.Phe345Ile
NM_001321910.1:c.1000T>A NP_001308839.1:p.Phe334Ile
NM_001321911.1:c.1000T>A NP_001308840.1:p.Phe334Ile
NM_001321912.1:c.1000T>A NP_001308841.1:p.Phe334Ile
NM_001321913.1:c.388T>A NP_001308842.1:p.Phe130Ile
NM_001321914.1:c.388T>A NP_001308843.1:p.Phe130Ile
NM_020868.4:c.1150T>A NP_065919.2:p.Phe384Ile
XM_017004566.1:c.1027T>A XP_016860055.1:p.Phe343Ile
XM_024453023.1:c.1090T>A XP_024308791.1:p.Phe364Ile
NM_001004360.4:c.1129T>A NP_001004360.3:p.Phe377Ile
NM_001178036.2:c.1000T>A NP_001171507.2:p.Phe334Ile
NM_001178037.2:c.1138T>A NP_001171508.2:p.Phe380Ile
NM_001321905.2:c.1201T>A NP_001308834.2:p.Phe401Ile
NM_001321907.2:c.1111T>A NP_001308836.2:p.Phe371Ile
NM_001321908.2:c.1060T>A NP_001308837.2:p.Phe354Ile
NM_001321909.2:c.1033T>A NP_001308838.2:p.Phe345Ile
NM_001321910.2:c.1000T>A NP_001308839.2:p.Phe334Ile
NM_001321911.2:c.1000T>A NP_001308840.2:p.Phe334Ile
NM_001321912.2:c.1000T>A NP_001308841.2:p.Phe334Ile
NM_001321913.2:c.388T>A NP_001308842.2:p.Phe130Ile
NM_020868.6:c.1150T>A MANE Select NP_065919.3:p.Phe384Ile
NM_001004360.5:c.1129T>A NP_001004360.3:p.Phe377Ile
NM_001178036.3:c.1000T>A NP_001171507.2:p.Phe334Ile
NM_001178037.3:c.1138T>A NP_001171508.2:p.Phe380Ile
NM_001321905.3:c.1201T>A NP_001308834.2:p.Phe401Ile
NM_001321906.2:c.1129T>A NP_001308835.2:p.Phe377Ile
NM_001321907.3:c.1111T>A NP_001308836.2:p.Phe371Ile
NM_001321908.3:c.1060T>A NP_001308837.2:p.Phe354Ile
NM_001321909.3:c.1033T>A NP_001308838.2:p.Phe345Ile
NM_001321910.3:c.1000T>A NP_001308839.2:p.Phe334Ile
NM_001321911.3:c.1000T>A NP_001308840.2:p.Phe334Ile
NM_001321912.3:c.1000T>A NP_001308841.2:p.Phe334Ile
NM_001321913.3:c.388T>A NP_001308842.2:p.Phe130Ile
NM_001321914.2:c.388T>A NP_001308843.2:p.Phe130Ile
NM_001399849.1:c.1000T>A NP_001386778.1:p.Phe334Ile
NM_001399850.1:c.388T>A NP_001386779.1:p.Phe130Ile
NM_001399851.1:c.898T>A NP_001386780.1:p.Phe300Ile