Canonical Allele Identifier: CA2660827067

Gene: DPP10

Linked Data

• gnomAD v4: 2-115768359-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768363_115768364dup , CM000664.2:g.115768363_115768364dup	GRCh38
NC_000002.11:g.116525939_116525940dup , CM000664.1:g.116525939_116525940dup	GRCh37
NC_000002.10:g.116242409_116242410dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410059.6:c.1180_1181dup MANE Select	ENSP00000386565.1:p.Arg395AspfsTer8
ENST00000310323.12:c.1159_1160dup	ENSP00000309066.8:p.Arg388AspfsTer8
ENST00000393147.6:c.1192_1193dup	ENSP00000376855.2:p.Arg399AspfsTer8
ENST00000409163.5:c.1030_1031dup	ENSP00000387038.1:p.Arg345AspfsTer8
ENST00000410059.5:c.1180_1181dup	ENSP00000386565.1:p.Arg395AspfsTer8
NM_001004360.3:c.1159_1160dup	NP_001004360.2:p.Arg388AspfsTer8
NM_001178034.1:c.1192_1193dup	NP_001171505.1:p.Arg399AspfsTer8
NM_001178036.1:c.1030_1031dup	NP_001171507.1:p.Arg345AspfsTer8
NM_001178037.1:c.1168_1169dup	NP_001171508.1:p.Arg391AspfsTer8
NM_020868.3:c.1180_1181dup	NP_065919.2:p.Arg395AspfsTer8
XM_011511526.1:c.1159_1160dup	XP_011509828.1:p.Arg388AspfsTer8
XM_011511527.1:c.1030_1031dup	XP_011509829.1:p.Arg345AspfsTer8
XM_011511528.1:c.928_929dup	XP_011509830.1:p.Arg311AspfsTer8
NM_001321905.1:c.1231_1232dup	NP_001308834.1:p.Arg412AspfsTer8
NM_001321906.1:c.1159_1160dup	NP_001308835.1:p.Arg388AspfsTer8
NM_001321907.1:c.1141_1142dup	NP_001308836.1:p.Arg382AspfsTer8
NM_001321908.1:c.1090_1091dup	NP_001308837.1:p.Arg365AspfsTer8
NM_001321909.1:c.1063_1064dup	NP_001308838.1:p.Arg356AspfsTer8
NM_001321910.1:c.1030_1031dup	NP_001308839.1:p.Arg345AspfsTer8
NM_001321911.1:c.1030_1031dup	NP_001308840.1:p.Arg345AspfsTer8
NM_001321912.1:c.1030_1031dup	NP_001308841.1:p.Arg345AspfsTer8
NM_001321913.1:c.418_419dup	NP_001308842.1:p.Arg141AspfsTer8
NM_001321914.1:c.418_419dup	NP_001308843.1:p.Arg141AspfsTer8
NM_020868.4:c.1180_1181dup	NP_065919.2:p.Arg395AspfsTer8
XM_017004566.1:c.1057_1058dup	XP_016860055.1:p.Arg354AspfsTer8
XM_024453023.1:c.1120_1121dup	XP_024308791.1:p.Arg375AspfsTer8
NM_001004360.4:c.1159_1160dup	NP_001004360.3:p.Arg388AspfsTer8
NM_001178036.2:c.1030_1031dup	NP_001171507.2:p.Arg345AspfsTer8
NM_001178037.2:c.1168_1169dup	NP_001171508.2:p.Arg391AspfsTer8
NM_001321905.2:c.1231_1232dup	NP_001308834.2:p.Arg412AspfsTer8
NM_001321907.2:c.1141_1142dup	NP_001308836.2:p.Arg382AspfsTer8
NM_001321908.2:c.1090_1091dup	NP_001308837.2:p.Arg365AspfsTer8
NM_001321909.2:c.1063_1064dup	NP_001308838.2:p.Arg356AspfsTer8
NM_001321910.2:c.1030_1031dup	NP_001308839.2:p.Arg345AspfsTer8
NM_001321911.2:c.1030_1031dup	NP_001308840.2:p.Arg345AspfsTer8
NM_001321912.2:c.1030_1031dup	NP_001308841.2:p.Arg345AspfsTer8
NM_001321913.2:c.418_419dup	NP_001308842.2:p.Arg141AspfsTer8
NM_020868.6:c.1180_1181dup MANE Select	NP_065919.3:p.Arg395AspfsTer8
NM_001004360.5:c.1159_1160dup	NP_001004360.3:p.Arg388AspfsTer8
NM_001178036.3:c.1030_1031dup	NP_001171507.2:p.Arg345AspfsTer8
NM_001178037.3:c.1168_1169dup	NP_001171508.2:p.Arg391AspfsTer8
NM_001321905.3:c.1231_1232dup	NP_001308834.2:p.Arg412AspfsTer8
NM_001321906.2:c.1159_1160dup	NP_001308835.2:p.Arg388AspfsTer8
NM_001321907.3:c.1141_1142dup	NP_001308836.2:p.Arg382AspfsTer8
NM_001321908.3:c.1090_1091dup	NP_001308837.2:p.Arg365AspfsTer8
NM_001321909.3:c.1063_1064dup	NP_001308838.2:p.Arg356AspfsTer8
NM_001321910.3:c.1030_1031dup	NP_001308839.2:p.Arg345AspfsTer8
NM_001321911.3:c.1030_1031dup	NP_001308840.2:p.Arg345AspfsTer8
NM_001321912.3:c.1030_1031dup	NP_001308841.2:p.Arg345AspfsTer8
NM_001321913.3:c.418_419dup	NP_001308842.2:p.Arg141AspfsTer8
NM_001321914.2:c.418_419dup	NP_001308843.2:p.Arg141AspfsTer8
NM_001399849.1:c.1030_1031dup	NP_001386778.1:p.Arg345AspfsTer8
NM_001399850.1:c.418_419dup	NP_001386779.1:p.Arg141AspfsTer8
NM_001399851.1:c.928_929dup	NP_001386780.1:p.Arg311AspfsTer8