Canonical Allele Identifier: CA348323423
Gene: DPP10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.115753200G>A , CM000664.2:g.115753200G>A GRCh38
NC_000002.11:g.116510776G>A , CM000664.1:g.116510776G>A GRCh37
NC_000002.10:g.116227246G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410059.6:c.977G>A MANE Select ENSP00000386565.1:p.Trp326Ter
ENST00000310323.12:c.956G>A ENSP00000309066.8:p.Trp319Ter
ENST00000393147.6:c.989G>A ENSP00000376855.2:p.Trp330Ter
ENST00000409163.5:c.827G>A ENSP00000387038.1:p.Trp276Ter
ENST00000410059.5:c.977G>A ENSP00000386565.1:p.Trp326Ter
NM_001004360.3:c.956G>A NP_001004360.2:p.Trp319Ter
NM_001178034.1:c.989G>A NP_001171505.1:p.Trp330Ter
NM_001178036.1:c.827G>A NP_001171507.1:p.Trp276Ter
NM_001178037.1:c.965G>A NP_001171508.1:p.Trp322Ter
NM_020868.3:c.977G>A NP_065919.2:p.Trp326Ter
XM_011511526.1:c.956G>A XP_011509828.1:p.Trp319Ter
XM_011511527.1:c.827G>A XP_011509829.1:p.Trp276Ter
XM_011511528.1:c.725G>A XP_011509830.1:p.Trp242Ter
XR_923234.1:n.67+1535C>T
NM_001321905.1:c.1028G>A NP_001308834.1:p.Trp343Ter
NM_001321906.1:c.956G>A NP_001308835.1:p.Trp319Ter
NM_001321907.1:c.977G>A NP_001308836.1:p.Trp326Ter
NM_001321908.1:c.887G>A NP_001308837.1:p.Trp296Ter
NM_001321909.1:c.860G>A NP_001308838.1:p.Trp287Ter
NM_001321910.1:c.827G>A NP_001308839.1:p.Trp276Ter
NM_001321911.1:c.827G>A NP_001308840.1:p.Trp276Ter
NM_001321912.1:c.827G>A NP_001308841.1:p.Trp276Ter
NM_001321913.1:c.215G>A NP_001308842.1:p.Trp72Ter
NM_001321914.1:c.215G>A NP_001308843.1:p.Trp72Ter
NM_020868.4:c.977G>A NP_065919.2:p.Trp326Ter
XM_017004566.1:c.854G>A XP_016860055.1:p.Trp285Ter
XM_024453023.1:c.956G>A XP_024308791.1:p.Trp319Ter
XR_923234.2:n.67+1535C>T
NM_001004360.4:c.956G>A NP_001004360.3:p.Trp319Ter
NM_001178036.2:c.827G>A NP_001171507.2:p.Trp276Ter
NM_001178037.2:c.965G>A NP_001171508.2:p.Trp322Ter
NM_001321905.2:c.1028G>A NP_001308834.2:p.Trp343Ter
NM_001321907.2:c.977G>A NP_001308836.2:p.Trp326Ter
NM_001321908.2:c.887G>A NP_001308837.2:p.Trp296Ter
NM_001321909.2:c.860G>A NP_001308838.2:p.Trp287Ter
NM_001321910.2:c.827G>A NP_001308839.2:p.Trp276Ter
NM_001321911.2:c.827G>A NP_001308840.2:p.Trp276Ter
NM_001321912.2:c.827G>A NP_001308841.2:p.Trp276Ter
NM_001321913.2:c.215G>A NP_001308842.2:p.Trp72Ter
NM_020868.6:c.977G>A MANE Select NP_065919.3:p.Trp326Ter
NM_001004360.5:c.956G>A NP_001004360.3:p.Trp319Ter
NM_001178036.3:c.827G>A NP_001171507.2:p.Trp276Ter
NM_001178037.3:c.965G>A NP_001171508.2:p.Trp322Ter
NM_001321905.3:c.1028G>A NP_001308834.2:p.Trp343Ter
NM_001321906.2:c.956G>A NP_001308835.2:p.Trp319Ter
NM_001321907.3:c.977G>A NP_001308836.2:p.Trp326Ter
NM_001321908.3:c.887G>A NP_001308837.2:p.Trp296Ter
NM_001321909.3:c.860G>A NP_001308838.2:p.Trp287Ter
NM_001321910.3:c.827G>A NP_001308839.2:p.Trp276Ter
NM_001321911.3:c.827G>A NP_001308840.2:p.Trp276Ter
NM_001321912.3:c.827G>A NP_001308841.2:p.Trp276Ter
NM_001321913.3:c.215G>A NP_001308842.2:p.Trp72Ter
NM_001321914.2:c.215G>A NP_001308843.2:p.Trp72Ter
NM_001399849.1:c.827G>A NP_001386778.1:p.Trp276Ter
NM_001399850.1:c.215G>A NP_001386779.1:p.Trp72Ter
NM_001399851.1:c.725G>A NP_001386780.1:p.Trp242Ter