Canonical Allele Identifier: CA1843103

Gene: DPP10

Linked Data

• dbSNP Id: rs142535149
• ExAC: 2:116525882 C / G
• gnomAD v2: 2-116525882-C-G
• gnomAD v3: 2-115768306-C-G
• gnomAD v4: 2-115768306-C-G
• MyVariant Identifiers: chr2:g.116525882C>G (hg19) ; chr2:g.115768306C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768306C>G , CM000664.2:g.115768306C>G	GRCh38
NC_000002.11:g.116525882C>G , CM000664.1:g.116525882C>G	GRCh37
NC_000002.10:g.116242352C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410059.6:c.1123C>G MANE Select	ENSP00000386565.1:p.Pro375Ala
ENST00000310323.12:c.1102C>G	ENSP00000309066.8:p.Pro368Ala
ENST00000393147.6:c.1135C>G	ENSP00000376855.2:p.Pro379Ala
ENST00000409163.5:c.973C>G	ENSP00000387038.1:p.Pro325Ala
ENST00000410059.5:c.1123C>G	ENSP00000386565.1:p.Pro375Ala
NM_001004360.3:c.1102C>G	NP_001004360.2:p.Pro368Ala
NM_001178034.1:c.1135C>G	NP_001171505.1:p.Pro379Ala
NM_001178036.1:c.973C>G	NP_001171507.1:p.Pro325Ala
NM_001178037.1:c.1111C>G	NP_001171508.1:p.Pro371Ala
NM_020868.3:c.1123C>G	NP_065919.2:p.Pro375Ala
XM_011511526.1:c.1102C>G	XP_011509828.1:p.Pro368Ala
XM_011511527.1:c.973C>G	XP_011509829.1:p.Pro325Ala
XM_011511528.1:c.871C>G	XP_011509830.1:p.Pro291Ala
NM_001321905.1:c.1174C>G	NP_001308834.1:p.Pro392Ala
NM_001321906.1:c.1102C>G	NP_001308835.1:p.Pro368Ala
NM_001321907.1:c.1084C>G	NP_001308836.1:p.Pro362Ala
NM_001321908.1:c.1033C>G	NP_001308837.1:p.Pro345Ala
NM_001321909.1:c.1006C>G	NP_001308838.1:p.Pro336Ala
NM_001321910.1:c.973C>G	NP_001308839.1:p.Pro325Ala
NM_001321911.1:c.973C>G	NP_001308840.1:p.Pro325Ala
NM_001321912.1:c.973C>G	NP_001308841.1:p.Pro325Ala
NM_001321913.1:c.361C>G	NP_001308842.1:p.Pro121Ala
NM_001321914.1:c.361C>G	NP_001308843.1:p.Pro121Ala
NM_020868.4:c.1123C>G	NP_065919.2:p.Pro375Ala
XM_017004566.1:c.1000C>G	XP_016860055.1:p.Pro334Ala
XM_024453023.1:c.1063C>G	XP_024308791.1:p.Pro355Ala
NM_001004360.4:c.1102C>G	NP_001004360.3:p.Pro368Ala
NM_001178036.2:c.973C>G	NP_001171507.2:p.Pro325Ala
NM_001178037.2:c.1111C>G	NP_001171508.2:p.Pro371Ala
NM_001321905.2:c.1174C>G	NP_001308834.2:p.Pro392Ala
NM_001321907.2:c.1084C>G	NP_001308836.2:p.Pro362Ala
NM_001321908.2:c.1033C>G	NP_001308837.2:p.Pro345Ala
NM_001321909.2:c.1006C>G	NP_001308838.2:p.Pro336Ala
NM_001321910.2:c.973C>G	NP_001308839.2:p.Pro325Ala
NM_001321911.2:c.973C>G	NP_001308840.2:p.Pro325Ala
NM_001321912.2:c.973C>G	NP_001308841.2:p.Pro325Ala
NM_001321913.2:c.361C>G	NP_001308842.2:p.Pro121Ala
NM_020868.6:c.1123C>G MANE Select	NP_065919.3:p.Pro375Ala
NM_001004360.5:c.1102C>G	NP_001004360.3:p.Pro368Ala
NM_001178036.3:c.973C>G	NP_001171507.2:p.Pro325Ala
NM_001178037.3:c.1111C>G	NP_001171508.2:p.Pro371Ala
NM_001321905.3:c.1174C>G	NP_001308834.2:p.Pro392Ala
NM_001321906.2:c.1102C>G	NP_001308835.2:p.Pro368Ala
NM_001321907.3:c.1084C>G	NP_001308836.2:p.Pro362Ala
NM_001321908.3:c.1033C>G	NP_001308837.2:p.Pro345Ala
NM_001321909.3:c.1006C>G	NP_001308838.2:p.Pro336Ala
NM_001321910.3:c.973C>G	NP_001308839.2:p.Pro325Ala
NM_001321911.3:c.973C>G	NP_001308840.2:p.Pro325Ala
NM_001321912.3:c.973C>G	NP_001308841.2:p.Pro325Ala
NM_001321913.3:c.361C>G	NP_001308842.2:p.Pro121Ala
NM_001321914.2:c.361C>G	NP_001308843.2:p.Pro121Ala
NM_001399849.1:c.973C>G	NP_001386778.1:p.Pro325Ala
NM_001399850.1:c.361C>G	NP_001386779.1:p.Pro121Ala
NM_001399851.1:c.871C>G	NP_001386780.1:p.Pro291Ala