Canonical Allele Identifier: CA428363075

Gene: DPP10

Linked Data

• gnomAD v4: 2-115768386-A-G
• MyVariant Identifiers: chr2:g.116525962A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768386A>G , CM000664.2:g.115768386A>G	GRCh38
NC_000002.11:g.116525962A>G , CM000664.1:g.116525962A>G	GRCh37
NC_000002.10:g.116242432A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410059.6:c.1203A>G MANE Select	ENSP00000386565.1:p.Val401=
ENST00000310323.12:c.1182A>G	ENSP00000309066.8:p.Val394=
ENST00000393147.6:c.1215A>G	ENSP00000376855.2:p.Val405=
ENST00000409163.5:c.1053A>G	ENSP00000387038.1:p.Val351=
ENST00000410059.5:c.1203A>G	ENSP00000386565.1:p.Val401=
NM_001004360.3:c.1182A>G	NP_001004360.2:p.Ile394Met
NM_001178034.1:c.1215A>G	NP_001171505.1:p.Ile405Met
NM_001178036.1:c.1053A>G	NP_001171507.1:p.Ile351Met
NM_001178037.1:c.1191A>G	NP_001171508.1:p.Ile397Met
NM_020868.3:c.1203A>G	NP_065919.2:p.Ile401Met
XM_011511526.1:c.1182A>G	XP_011509828.1:p.Val394=
XM_011511527.1:c.1053A>G	XP_011509829.1:p.Val351=
XM_011511528.1:c.951A>G	XP_011509830.1:p.Val317=
NM_001321905.1:c.1254A>G	NP_001308834.1:p.Ile418Met
NM_001321906.1:c.1182A>G	NP_001308835.1:p.Ile394Met
NM_001321907.1:c.1164A>G	NP_001308836.1:p.Ile388Met
NM_001321908.1:c.1113A>G	NP_001308837.1:p.Ile371Met
NM_001321909.1:c.1086A>G	NP_001308838.1:p.Ile362Met
NM_001321910.1:c.1053A>G	NP_001308839.1:p.Ile351Met
NM_001321911.1:c.1053A>G	NP_001308840.1:p.Ile351Met
NM_001321912.1:c.1053A>G	NP_001308841.1:p.Ile351Met
NM_001321913.1:c.441A>G	NP_001308842.1:p.Ile147Met
NM_001321914.1:c.441A>G	NP_001308843.1:p.Ile147Met
NM_020868.4:c.1203A>G	NP_065919.2:p.Ile401Met
XM_017004566.1:c.1080A>G	XP_016860055.1:p.Val360=
XM_024453023.1:c.1143A>G	XP_024308791.1:p.Val381=
NM_001004360.4:c.1182A>G	NP_001004360.3:p.Val394=
NM_001178036.2:c.1053A>G	NP_001171507.2:p.Val351=
NM_001178037.2:c.1191A>G	NP_001171508.2:p.Val397=
NM_001321905.2:c.1254A>G	NP_001308834.2:p.Val418=
NM_001321907.2:c.1164A>G	NP_001308836.2:p.Val388=
NM_001321908.2:c.1113A>G	NP_001308837.2:p.Val371=
NM_001321909.2:c.1086A>G	NP_001308838.2:p.Val362=
NM_001321910.2:c.1053A>G	NP_001308839.2:p.Val351=
NM_001321911.2:c.1053A>G	NP_001308840.2:p.Val351=
NM_001321912.2:c.1053A>G	NP_001308841.2:p.Val351=
NM_001321913.2:c.441A>G	NP_001308842.2:p.Val147=
NM_020868.6:c.1203A>G MANE Select	NP_065919.3:p.Val401=
NM_001004360.5:c.1182A>G	NP_001004360.3:p.Val394=
NM_001178036.3:c.1053A>G	NP_001171507.2:p.Val351=
NM_001178037.3:c.1191A>G	NP_001171508.2:p.Val397=
NM_001321905.3:c.1254A>G	NP_001308834.2:p.Val418=
NM_001321906.2:c.1182A>G	NP_001308835.2:p.Val394=
NM_001321907.3:c.1164A>G	NP_001308836.2:p.Val388=
NM_001321908.3:c.1113A>G	NP_001308837.2:p.Val371=
NM_001321909.3:c.1086A>G	NP_001308838.2:p.Val362=
NM_001321910.3:c.1053A>G	NP_001308839.2:p.Val351=
NM_001321911.3:c.1053A>G	NP_001308840.2:p.Val351=
NM_001321912.3:c.1053A>G	NP_001308841.2:p.Val351=
NM_001321913.3:c.441A>G	NP_001308842.2:p.Val147=
NM_001321914.2:c.441A>G	NP_001308843.2:p.Val147=
NM_001399849.1:c.1053A>G	NP_001386778.1:p.Val351=
NM_001399850.1:c.441A>G	NP_001386779.1:p.Val147=
NM_001399851.1:c.951A>G	NP_001386780.1:p.Val317=