Canonical Allele Identifier: CA2840702507

Gene: DPP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115753324G>T , CM000664.2:g.115753324G>T	GRCh38
NC_000002.11:g.116510900G>T , CM000664.1:g.116510900G>T	GRCh37
NC_000002.10:g.116227370G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410059.6:c.1074+27G>T MANE Select	ENSP00000386565.1:n.1074+27G>T
ENST00000310323.12:c.1053+27G>T	ENSP00000309066.8:n.1053+27G>T
ENST00000393147.6:c.1086+27G>T	ENSP00000376855.2:n.1086+27G>T
ENST00000409163.5:c.924+27G>T	ENSP00000387038.1:n.924+27G>T
ENST00000410059.5:c.1074+27G>T	ENSP00000386565.1:n.1074+27G>T
NM_001004360.3:c.1053+27G>T	NP_001004360.2:n.1053+27G>T
NM_001178034.1:c.1086+27G>T	NP_001171505.1:n.1086+27G>T
NM_001178036.1:c.924+27G>T	NP_001171507.1:n.924+27G>T
NM_001178037.1:c.1062+27G>T	NP_001171508.1:n.1062+27G>T
NM_020868.3:c.1074+27G>T	NP_065919.2:n.1074+27G>T
XM_011511526.1:c.1053+27G>T	XP_011509828.1:n.1053+27G>T
XM_011511527.1:c.924+27G>T	XP_011509829.1:n.924+27G>T
XM_011511528.1:c.822+27G>T	XP_011509830.1:n.822+27G>T
XR_923234.1:n.67+1411C>A
NM_001321905.1:c.1125+27G>T	NP_001308834.1:n.1125+27G>T
NM_001321906.1:c.1053+27G>T	NP_001308835.1:n.1053+27G>T
NM_001321907.1:c.1074+27G>T	NP_001308836.1:n.1074+27G>T
NM_001321908.1:c.984+27G>T	NP_001308837.1:n.984+27G>T
NM_001321909.1:c.957+27G>T	NP_001308838.1:n.957+27G>T
NM_001321910.1:c.924+27G>T	NP_001308839.1:n.924+27G>T
NM_001321911.1:c.924+27G>T	NP_001308840.1:n.924+27G>T
NM_001321912.1:c.924+27G>T	NP_001308841.1:n.924+27G>T
NM_001321913.1:c.312+27G>T	NP_001308842.1:n.312+27G>T
NM_001321914.1:c.312+27G>T	NP_001308843.1:n.312+27G>T
NM_020868.4:c.1074+27G>T	NP_065919.2:n.1074+27G>T
XM_017004566.1:c.951+27G>T	XP_016860055.1:n.951+27G>T
XM_024453023.1:c.1053+27G>T	XP_024308791.1:n.1053+27G>T
XR_923234.2:n.67+1411C>A
NM_001004360.4:c.1053+27G>T	NP_001004360.3:n.1053+27G>T
NM_001178036.2:c.924+27G>T	NP_001171507.2:n.924+27G>T
NM_001178037.2:c.1062+27G>T	NP_001171508.2:n.1062+27G>T
NM_001321905.2:c.1125+27G>T	NP_001308834.2:n.1125+27G>T
NM_001321907.2:c.1074+27G>T	NP_001308836.2:n.1074+27G>T
NM_001321908.2:c.984+27G>T	NP_001308837.2:n.984+27G>T
NM_001321909.2:c.957+27G>T	NP_001308838.2:n.957+27G>T
NM_001321910.2:c.924+27G>T	NP_001308839.2:n.924+27G>T
NM_001321911.2:c.924+27G>T	NP_001308840.2:n.924+27G>T
NM_001321912.2:c.924+27G>T	NP_001308841.2:n.924+27G>T
NM_001321913.2:c.312+27G>T	NP_001308842.2:n.312+27G>T
NM_020868.6:c.1074+27G>T MANE Select	NP_065919.3:n.1074+27G>T
NM_001004360.5:c.1053+27G>T	NP_001004360.3:n.1053+27G>T
NM_001178036.3:c.924+27G>T	NP_001171507.2:n.924+27G>T
NM_001178037.3:c.1062+27G>T	NP_001171508.2:n.1062+27G>T
NM_001321905.3:c.1125+27G>T	NP_001308834.2:n.1125+27G>T
NM_001321906.2:c.1053+27G>T	NP_001308835.2:n.1053+27G>T
NM_001321907.3:c.1074+27G>T	NP_001308836.2:n.1074+27G>T
NM_001321908.3:c.984+27G>T	NP_001308837.2:n.984+27G>T
NM_001321909.3:c.957+27G>T	NP_001308838.2:n.957+27G>T
NM_001321910.3:c.924+27G>T	NP_001308839.2:n.924+27G>T
NM_001321911.3:c.924+27G>T	NP_001308840.2:n.924+27G>T
NM_001321912.3:c.924+27G>T	NP_001308841.2:n.924+27G>T
NM_001321913.3:c.312+27G>T	NP_001308842.2:n.312+27G>T
NM_001321914.2:c.312+27G>T	NP_001308843.2:n.312+27G>T
NM_001399849.1:c.924+27G>T	NP_001386778.1:n.924+27G>T
NM_001399850.1:c.312+27G>T	NP_001386779.1:n.312+27G>T
NM_001399851.1:c.822+27G>T	NP_001386780.1:n.822+27G>T