Canonical Allele Identifier: CA428354265

Gene: DPP10

Linked Data

• dbSNP Id: rs1223303709
• gnomAD v2: 2-116510762-C-T
• gnomAD v4: 2-115753186-C-T
• MyVariant Identifiers: chr2:g.116510762C>T (hg19) ; chr2:g.115753186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115753186C>T , CM000664.2:g.115753186C>T	GRCh38
NC_000002.11:g.116510762C>T , CM000664.1:g.116510762C>T	GRCh37
NC_000002.10:g.116227232C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410059.6:c.963C>T MANE Select	ENSP00000386565.1:p.Ile321=
ENST00000310323.12:c.942C>T	ENSP00000309066.8:p.Ile314=
ENST00000393147.6:c.975C>T	ENSP00000376855.2:p.Ile325=
ENST00000409163.5:c.813C>T	ENSP00000387038.1:p.Ile271=
ENST00000410059.5:c.963C>T	ENSP00000386565.1:p.Ile321=
NM_001004360.3:c.942C>T	NP_001004360.2:p.Ile314=
NM_001178034.1:c.975C>T	NP_001171505.1:p.Ile325=
NM_001178036.1:c.813C>T	NP_001171507.1:p.Ile271=
NM_001178037.1:c.951C>T	NP_001171508.1:p.Ile317=
NM_020868.3:c.963C>T	NP_065919.2:p.Ile321=
XM_011511526.1:c.942C>T	XP_011509828.1:p.Ile314=
XM_011511527.1:c.813C>T	XP_011509829.1:p.Ile271=
XM_011511528.1:c.711C>T	XP_011509830.1:p.Ile237=
XR_923234.1:n.67+1549G>A
NM_001321905.1:c.1014C>T	NP_001308834.1:p.Ile338=
NM_001321906.1:c.942C>T	NP_001308835.1:p.Ile314=
NM_001321907.1:c.963C>T	NP_001308836.1:p.Ile321=
NM_001321908.1:c.873C>T	NP_001308837.1:p.Ile291=
NM_001321909.1:c.846C>T	NP_001308838.1:p.Ile282=
NM_001321910.1:c.813C>T	NP_001308839.1:p.Ile271=
NM_001321911.1:c.813C>T	NP_001308840.1:p.Ile271=
NM_001321912.1:c.813C>T	NP_001308841.1:p.Ile271=
NM_001321913.1:c.201C>T	NP_001308842.1:p.Ile67=
NM_001321914.1:c.201C>T	NP_001308843.1:p.Ile67=
NM_020868.4:c.963C>T	NP_065919.2:p.Ile321=
XM_017004566.1:c.840C>T	XP_016860055.1:p.Ile280=
XM_024453023.1:c.942C>T	XP_024308791.1:p.Ile314=
XR_923234.2:n.67+1549G>A
NM_001004360.4:c.942C>T	NP_001004360.3:p.Ile314=
NM_001178036.2:c.813C>T	NP_001171507.2:p.Ile271=
NM_001178037.2:c.951C>T	NP_001171508.2:p.Ile317=
NM_001321905.2:c.1014C>T	NP_001308834.2:p.Ile338=
NM_001321907.2:c.963C>T	NP_001308836.2:p.Ile321=
NM_001321908.2:c.873C>T	NP_001308837.2:p.Ile291=
NM_001321909.2:c.846C>T	NP_001308838.2:p.Ile282=
NM_001321910.2:c.813C>T	NP_001308839.2:p.Ile271=
NM_001321911.2:c.813C>T	NP_001308840.2:p.Ile271=
NM_001321912.2:c.813C>T	NP_001308841.2:p.Ile271=
NM_001321913.2:c.201C>T	NP_001308842.2:p.Ile67=
NM_020868.6:c.963C>T MANE Select	NP_065919.3:p.Ile321=
NM_001004360.5:c.942C>T	NP_001004360.3:p.Ile314=
NM_001178036.3:c.813C>T	NP_001171507.2:p.Ile271=
NM_001178037.3:c.951C>T	NP_001171508.2:p.Ile317=
NM_001321905.3:c.1014C>T	NP_001308834.2:p.Ile338=
NM_001321906.2:c.942C>T	NP_001308835.2:p.Ile314=
NM_001321907.3:c.963C>T	NP_001308836.2:p.Ile321=
NM_001321908.3:c.873C>T	NP_001308837.2:p.Ile291=
NM_001321909.3:c.846C>T	NP_001308838.2:p.Ile282=
NM_001321910.3:c.813C>T	NP_001308839.2:p.Ile271=
NM_001321911.3:c.813C>T	NP_001308840.2:p.Ile271=
NM_001321912.3:c.813C>T	NP_001308841.2:p.Ile271=
NM_001321913.3:c.201C>T	NP_001308842.2:p.Ile67=
NM_001321914.2:c.201C>T	NP_001308843.2:p.Ile67=
NM_001399849.1:c.813C>T	NP_001386778.1:p.Ile271=
NM_001399850.1:c.201C>T	NP_001386779.1:p.Ile67=
NM_001399851.1:c.711C>T	NP_001386780.1:p.Ile237=