Canonical Allele Identifier: CA1843119

Gene: DPP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768384G>A , CM000664.2:g.115768384G>A	GRCh38
NC_000002.11:g.116525960G>A , CM000664.1:g.116525960G>A	GRCh37
NC_000002.10:g.116242430G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020868.6:c.1201G>A MANE Select	NP_065919.3:p.Val401Ile
ENST00000410059.6:c.1201G>A MANE Select	ENSP00000386565.1:p.Val401Ile
NM_001004360.4:c.1180G>A	NP_001004360.3:p.Val394Ile
NM_001004360.5:c.1180G>A	NP_001004360.3:p.Val394Ile
NM_001178036.2:c.1051G>A	NP_001171507.2:p.Val351Ile
NM_001178036.3:c.1051G>A	NP_001171507.2:p.Val351Ile
NM_001178037.2:c.1189G>A	NP_001171508.2:p.Val397Ile
NM_001178037.3:c.1189G>A	NP_001171508.2:p.Val397Ile
NM_001321905.2:c.1252G>A	NP_001308834.2:p.Val418Ile
NM_001321905.3:c.1252G>A	NP_001308834.2:p.Val418Ile
NM_001321906.2:c.1180G>A	NP_001308835.2:p.Val394Ile
NM_001321907.2:c.1162G>A	NP_001308836.2:p.Val388Ile
NM_001321907.3:c.1162G>A	NP_001308836.2:p.Val388Ile
NM_001321908.2:c.1111G>A	NP_001308837.2:p.Val371Ile
NM_001321908.3:c.1111G>A	NP_001308837.2:p.Val371Ile
NM_001321909.2:c.1084G>A	NP_001308838.2:p.Val362Ile
NM_001321909.3:c.1084G>A	NP_001308838.2:p.Val362Ile
NM_001321910.2:c.1051G>A	NP_001308839.2:p.Val351Ile
NM_001321910.3:c.1051G>A	NP_001308839.2:p.Val351Ile
NM_001321911.2:c.1051G>A	NP_001308840.2:p.Val351Ile
NM_001321911.3:c.1051G>A	NP_001308840.2:p.Val351Ile
NM_001321912.2:c.1051G>A	NP_001308841.2:p.Val351Ile
NM_001321912.3:c.1051G>A	NP_001308841.2:p.Val351Ile
NM_001321913.2:c.439G>A	NP_001308842.2:p.Val147Ile
NM_001321913.3:c.439G>A	NP_001308842.2:p.Val147Ile
NM_001321914.2:c.439G>A	NP_001308843.2:p.Val147Ile
NM_001399849.1:c.1051G>A	NP_001386778.1:p.Val351Ile
NM_001399850.1:c.439G>A	NP_001386779.1:p.Val147Ile
NM_001399851.1:c.949G>A	NP_001386780.1:p.Val317Ile
ENST00000310323.12:c.1180G>A	ENSP00000309066.8:p.Val394Ile
ENST00000393147.6:c.1213G>A	ENSP00000376855.2:p.Val405Ile
ENST00000409163.5:c.1051G>A	ENSP00000387038.1:p.Val351Ile
ENST00000410059.5:c.1201G>A	ENSP00000386565.1:p.Val401Ile
XM_011511526.1:c.1180G>A	XP_011509828.1:p.Val394Ile
XM_011511527.1:c.1051G>A	XP_011509829.1:p.Val351Ile
XM_011511528.1:c.949G>A	XP_011509830.1:p.Val317Ile
XM_017004566.1:c.1078G>A	XP_016860055.1:p.Val360Ile
XM_024453023.1:c.1141G>A	XP_024308791.1:p.Val381Ile