Canonical Allele Identifier: CA348324537

Gene: DPP10

Linked Data

• gnomAD v4: 2-115768391-T-C
• MyVariant Identifiers: chr2:g.116525967T>C (hg19) ; chr2:g.115768391T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768391T>C , CM000664.2:g.115768391T>C	GRCh38
NC_000002.11:g.116525967T>C , CM000664.1:g.116525967T>C	GRCh37
NC_000002.10:g.116242437T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410059.6:c.1208T>C MANE Select	ENSP00000386565.1:p.Met403Thr
ENST00000310323.12:c.1187T>C	ENSP00000309066.8:p.Met396Thr
ENST00000393147.6:c.1220T>C	ENSP00000376855.2:p.Met407Thr
ENST00000409163.5:c.1058T>C	ENSP00000387038.1:p.Met353Thr
ENST00000410059.5:c.1208T>C	ENSP00000386565.1:p.Met403Thr
NM_001004360.3:c.1187T>C	NP_001004360.2:p.Met396Thr
NM_001178034.1:c.1220T>C	NP_001171505.1:p.Met407Thr
NM_001178036.1:c.1058T>C	NP_001171507.1:p.Met353Thr
NM_001178037.1:c.1196T>C	NP_001171508.1:p.Met399Thr
NM_020868.3:c.1208T>C	NP_065919.2:p.Met403Thr
XM_011511526.1:c.1187T>C	XP_011509828.1:p.Met396Thr
XM_011511527.1:c.1058T>C	XP_011509829.1:p.Met353Thr
XM_011511528.1:c.956T>C	XP_011509830.1:p.Met319Thr
NM_001321905.1:c.1259T>C	NP_001308834.1:p.Met420Thr
NM_001321906.1:c.1187T>C	NP_001308835.1:p.Met396Thr
NM_001321907.1:c.1169T>C	NP_001308836.1:p.Met390Thr
NM_001321908.1:c.1118T>C	NP_001308837.1:p.Met373Thr
NM_001321909.1:c.1091T>C	NP_001308838.1:p.Met364Thr
NM_001321910.1:c.1058T>C	NP_001308839.1:p.Met353Thr
NM_001321911.1:c.1058T>C	NP_001308840.1:p.Met353Thr
NM_001321912.1:c.1058T>C	NP_001308841.1:p.Met353Thr
NM_001321913.1:c.446T>C	NP_001308842.1:p.Met149Thr
NM_001321914.1:c.446T>C	NP_001308843.1:p.Met149Thr
NM_020868.4:c.1208T>C	NP_065919.2:p.Met403Thr
XM_017004566.1:c.1085T>C	XP_016860055.1:p.Met362Thr
XM_024453023.1:c.1148T>C	XP_024308791.1:p.Met383Thr
NM_001004360.4:c.1187T>C	NP_001004360.3:p.Met396Thr
NM_001178036.2:c.1058T>C	NP_001171507.2:p.Met353Thr
NM_001178037.2:c.1196T>C	NP_001171508.2:p.Met399Thr
NM_001321905.2:c.1259T>C	NP_001308834.2:p.Met420Thr
NM_001321907.2:c.1169T>C	NP_001308836.2:p.Met390Thr
NM_001321908.2:c.1118T>C	NP_001308837.2:p.Met373Thr
NM_001321909.2:c.1091T>C	NP_001308838.2:p.Met364Thr
NM_001321910.2:c.1058T>C	NP_001308839.2:p.Met353Thr
NM_001321911.2:c.1058T>C	NP_001308840.2:p.Met353Thr
NM_001321912.2:c.1058T>C	NP_001308841.2:p.Met353Thr
NM_001321913.2:c.446T>C	NP_001308842.2:p.Met149Thr
NM_020868.6:c.1208T>C MANE Select	NP_065919.3:p.Met403Thr
NM_001004360.5:c.1187T>C	NP_001004360.3:p.Met396Thr
NM_001178036.3:c.1058T>C	NP_001171507.2:p.Met353Thr
NM_001178037.3:c.1196T>C	NP_001171508.2:p.Met399Thr
NM_001321905.3:c.1259T>C	NP_001308834.2:p.Met420Thr
NM_001321906.2:c.1187T>C	NP_001308835.2:p.Met396Thr
NM_001321907.3:c.1169T>C	NP_001308836.2:p.Met390Thr
NM_001321908.3:c.1118T>C	NP_001308837.2:p.Met373Thr
NM_001321909.3:c.1091T>C	NP_001308838.2:p.Met364Thr
NM_001321910.3:c.1058T>C	NP_001308839.2:p.Met353Thr
NM_001321911.3:c.1058T>C	NP_001308840.2:p.Met353Thr
NM_001321912.3:c.1058T>C	NP_001308841.2:p.Met353Thr
NM_001321913.3:c.446T>C	NP_001308842.2:p.Met149Thr
NM_001321914.2:c.446T>C	NP_001308843.2:p.Met149Thr
NM_001399849.1:c.1058T>C	NP_001386778.1:p.Met353Thr
NM_001399850.1:c.446T>C	NP_001386779.1:p.Met149Thr
NM_001399851.1:c.956T>C	NP_001386780.1:p.Met319Thr