Canonical Allele Identifier: CA1281319705

Gene: DPP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768342A= , CM000664.2:g.115768342A=	GRCh38
NC_000002.11:g.116525918A= , CM000664.1:g.116525918A=	GRCh37
NC_000002.10:g.116242388A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410059.6:c.1159A= MANE Select	ENSP00000386565.1:p.Thr387=
ENST00000310323.12:c.1138A=	ENSP00000309066.8:p.Thr380=
ENST00000393147.6:c.1171A=	ENSP00000376855.2:p.Thr391=
ENST00000409163.5:c.1009A=	ENSP00000387038.1:p.Thr337=
ENST00000410059.5:c.1159A=	ENSP00000386565.1:p.Thr387=
NM_001004360.3:c.1138A=	NP_001004360.2:p.Thr380=
NM_001178034.1:c.1171A=	NP_001171505.1:p.Thr391=
NM_001178036.1:c.1009A=	NP_001171507.1:p.Thr337=
NM_001178037.1:c.1147A=	NP_001171508.1:p.Thr383=
NM_020868.3:c.1159A=	NP_065919.2:p.Thr387=
XM_011511526.1:c.1138A=	XP_011509828.1:p.Thr380=
XM_011511527.1:c.1009A=	XP_011509829.1:p.Thr337=
XM_011511528.1:c.907A=	XP_011509830.1:p.Thr303=
NM_001321905.1:c.1210A=	NP_001308834.1:p.Thr404=
NM_001321906.1:c.1138A=	NP_001308835.1:p.Thr380=
NM_001321907.1:c.1120A=	NP_001308836.1:p.Thr374=
NM_001321908.1:c.1069A=	NP_001308837.1:p.Thr357=
NM_001321909.1:c.1042A=	NP_001308838.1:p.Thr348=
NM_001321910.1:c.1009A=	NP_001308839.1:p.Thr337=
NM_001321911.1:c.1009A=	NP_001308840.1:p.Thr337=
NM_001321912.1:c.1009A=	NP_001308841.1:p.Thr337=
NM_001321913.1:c.397A=	NP_001308842.1:p.Thr133=
NM_001321914.1:c.397A=	NP_001308843.1:p.Thr133=
NM_020868.4:c.1159A=	NP_065919.2:p.Thr387=
XM_017004566.1:c.1036A=	XP_016860055.1:p.Thr346=
XM_024453023.1:c.1099A=	XP_024308791.1:p.Thr367=
NM_001004360.4:c.1138A=	NP_001004360.3:p.Thr380=
NM_001178036.2:c.1009A=	NP_001171507.2:p.Thr337=
NM_001178037.2:c.1147A=	NP_001171508.2:p.Thr383=
NM_001321905.2:c.1210A=	NP_001308834.2:p.Thr404=
NM_001321907.2:c.1120A=	NP_001308836.2:p.Thr374=
NM_001321908.2:c.1069A=	NP_001308837.2:p.Thr357=
NM_001321909.2:c.1042A=	NP_001308838.2:p.Thr348=
NM_001321910.2:c.1009A=	NP_001308839.2:p.Thr337=
NM_001321911.2:c.1009A=	NP_001308840.2:p.Thr337=
NM_001321912.2:c.1009A=	NP_001308841.2:p.Thr337=
NM_001321913.2:c.397A=	NP_001308842.2:p.Thr133=
NM_020868.6:c.1159A= MANE Select	NP_065919.3:p.Thr387=
NM_001004360.5:c.1138A=	NP_001004360.3:p.Thr380=
NM_001178036.3:c.1009A=	NP_001171507.2:p.Thr337=
NM_001178037.3:c.1147A=	NP_001171508.2:p.Thr383=
NM_001321905.3:c.1210A=	NP_001308834.2:p.Thr404=
NM_001321906.2:c.1138A=	NP_001308835.2:p.Thr380=
NM_001321907.3:c.1120A=	NP_001308836.2:p.Thr374=
NM_001321908.3:c.1069A=	NP_001308837.2:p.Thr357=
NM_001321909.3:c.1042A=	NP_001308838.2:p.Thr348=
NM_001321910.3:c.1009A=	NP_001308839.2:p.Thr337=
NM_001321911.3:c.1009A=	NP_001308840.2:p.Thr337=
NM_001321912.3:c.1009A=	NP_001308841.2:p.Thr337=
NM_001321913.3:c.397A=	NP_001308842.2:p.Thr133=
NM_001321914.2:c.397A=	NP_001308843.2:p.Thr133=
NM_001399849.1:c.1009A=	NP_001386778.1:p.Thr337=
NM_001399850.1:c.397A=	NP_001386779.1:p.Thr133=
NM_001399851.1:c.907A=	NP_001386780.1:p.Thr303=