Canonical Allele Identifier: CA2660827066

Gene: DPP10

Linked Data

• gnomAD v4: 2-115768336-TTTATGACAGTGCCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768340_115768354del , CM000664.2:g.115768340_115768354del	GRCh38
NC_000002.11:g.116525916_116525930del , CM000664.1:g.116525916_116525930del	GRCh37
NC_000002.10:g.116242386_116242400del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410059.6:c.1157_1171del MANE Select	ENSP00000386565.1:p.Met386_Val390del
ENST00000310323.12:c.1136_1150del	ENSP00000309066.8:p.Met379_Val383del
ENST00000393147.6:c.1169_1183del	ENSP00000376855.2:p.Met390_Val394del
ENST00000409163.5:c.1007_1021del	ENSP00000387038.1:p.Met336_Val340del
ENST00000410059.5:c.1157_1171del	ENSP00000386565.1:p.Met386_Val390del
NM_001004360.3:c.1136_1150del	NP_001004360.2:p.Met379_Val383del
NM_001178034.1:c.1169_1183del	NP_001171505.1:p.Met390_Val394del
NM_001178036.1:c.1007_1021del	NP_001171507.1:p.Met336_Val340del
NM_001178037.1:c.1145_1159del	NP_001171508.1:p.Met382_Val386del
NM_020868.3:c.1157_1171del	NP_065919.2:p.Met386_Val390del
XM_011511526.1:c.1136_1150del	XP_011509828.1:p.Met379_Val383del
XM_011511527.1:c.1007_1021del	XP_011509829.1:p.Met336_Val340del
XM_011511528.1:c.905_919del	XP_011509830.1:p.Met302_Val306del
NM_001321905.1:c.1208_1222del	NP_001308834.1:p.Met403_Val407del
NM_001321906.1:c.1136_1150del	NP_001308835.1:p.Met379_Val383del
NM_001321907.1:c.1118_1132del	NP_001308836.1:p.Met373_Val377del
NM_001321908.1:c.1067_1081del	NP_001308837.1:p.Met356_Val360del
NM_001321909.1:c.1040_1054del	NP_001308838.1:p.Met347_Val351del
NM_001321910.1:c.1007_1021del	NP_001308839.1:p.Met336_Val340del
NM_001321911.1:c.1007_1021del	NP_001308840.1:p.Met336_Val340del
NM_001321912.1:c.1007_1021del	NP_001308841.1:p.Met336_Val340del
NM_001321913.1:c.395_409del	NP_001308842.1:p.Met132_Val136del
NM_001321914.1:c.395_409del	NP_001308843.1:p.Met132_Val136del
NM_020868.4:c.1157_1171del	NP_065919.2:p.Met386_Val390del
XM_017004566.1:c.1034_1048del	XP_016860055.1:p.Met345_Val349del
XM_024453023.1:c.1097_1111del	XP_024308791.1:p.Met366_Val370del
NM_001004360.4:c.1136_1150del	NP_001004360.3:p.Met379_Val383del
NM_001178036.2:c.1007_1021del	NP_001171507.2:p.Met336_Val340del
NM_001178037.2:c.1145_1159del	NP_001171508.2:p.Met382_Val386del
NM_001321905.2:c.1208_1222del	NP_001308834.2:p.Met403_Val407del
NM_001321907.2:c.1118_1132del	NP_001308836.2:p.Met373_Val377del
NM_001321908.2:c.1067_1081del	NP_001308837.2:p.Met356_Val360del
NM_001321909.2:c.1040_1054del	NP_001308838.2:p.Met347_Val351del
NM_001321910.2:c.1007_1021del	NP_001308839.2:p.Met336_Val340del
NM_001321911.2:c.1007_1021del	NP_001308840.2:p.Met336_Val340del
NM_001321912.2:c.1007_1021del	NP_001308841.2:p.Met336_Val340del
NM_001321913.2:c.395_409del	NP_001308842.2:p.Met132_Val136del
NM_020868.6:c.1157_1171del MANE Select	NP_065919.3:p.Met386_Val390del
NM_001004360.5:c.1136_1150del	NP_001004360.3:p.Met379_Val383del
NM_001178036.3:c.1007_1021del	NP_001171507.2:p.Met336_Val340del
NM_001178037.3:c.1145_1159del	NP_001171508.2:p.Met382_Val386del
NM_001321905.3:c.1208_1222del	NP_001308834.2:p.Met403_Val407del
NM_001321906.2:c.1136_1150del	NP_001308835.2:p.Met379_Val383del
NM_001321907.3:c.1118_1132del	NP_001308836.2:p.Met373_Val377del
NM_001321908.3:c.1067_1081del	NP_001308837.2:p.Met356_Val360del
NM_001321909.3:c.1040_1054del	NP_001308838.2:p.Met347_Val351del
NM_001321910.3:c.1007_1021del	NP_001308839.2:p.Met336_Val340del
NM_001321911.3:c.1007_1021del	NP_001308840.2:p.Met336_Val340del
NM_001321912.3:c.1007_1021del	NP_001308841.2:p.Met336_Val340del
NM_001321913.3:c.395_409del	NP_001308842.2:p.Met132_Val136del
NM_001321914.2:c.395_409del	NP_001308843.2:p.Met132_Val136del
NM_001399849.1:c.1007_1021del	NP_001386778.1:p.Met336_Val340del
NM_001399850.1:c.395_409del	NP_001386779.1:p.Met132_Val136del
NM_001399851.1:c.905_919del	NP_001386780.1:p.Met302_Val306del