Canonical Allele Identifier: CA348323571

Gene: DPP10

Linked Data

• gnomAD v4: 2-115753266-T-A
• MyVariant Identifiers: chr2:g.116510842T>A (hg19) ; chr2:g.115753266T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115753266T>A , CM000664.2:g.115753266T>A	GRCh38
NC_000002.11:g.116510842T>A , CM000664.1:g.116510842T>A	GRCh37
NC_000002.10:g.116227312T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410059.6:c.1043T>A MANE Select	ENSP00000386565.1:p.Val348Asp
ENST00000310323.12:c.1022T>A	ENSP00000309066.8:p.Val341Asp
ENST00000393147.6:c.1055T>A	ENSP00000376855.2:p.Val352Asp
ENST00000409163.5:c.893T>A	ENSP00000387038.1:p.Val298Asp
ENST00000410059.5:c.1043T>A	ENSP00000386565.1:p.Val348Asp
NM_001004360.3:c.1022T>A	NP_001004360.2:p.Val341Asp
NM_001178034.1:c.1055T>A	NP_001171505.1:p.Val352Asp
NM_001178036.1:c.893T>A	NP_001171507.1:p.Val298Asp
NM_001178037.1:c.1031T>A	NP_001171508.1:p.Val344Asp
NM_020868.3:c.1043T>A	NP_065919.2:p.Val348Asp
XM_011511526.1:c.1022T>A	XP_011509828.1:p.Val341Asp
XM_011511527.1:c.893T>A	XP_011509829.1:p.Val298Asp
XM_011511528.1:c.791T>A	XP_011509830.1:p.Val264Asp
XR_923234.1:n.67+1469A>T
NM_001321905.1:c.1094T>A	NP_001308834.1:p.Val365Asp
NM_001321906.1:c.1022T>A	NP_001308835.1:p.Val341Asp
NM_001321907.1:c.1043T>A	NP_001308836.1:p.Val348Asp
NM_001321908.1:c.953T>A	NP_001308837.1:p.Val318Asp
NM_001321909.1:c.926T>A	NP_001308838.1:p.Val309Asp
NM_001321910.1:c.893T>A	NP_001308839.1:p.Val298Asp
NM_001321911.1:c.893T>A	NP_001308840.1:p.Val298Asp
NM_001321912.1:c.893T>A	NP_001308841.1:p.Val298Asp
NM_001321913.1:c.281T>A	NP_001308842.1:p.Val94Asp
NM_001321914.1:c.281T>A	NP_001308843.1:p.Val94Asp
NM_020868.4:c.1043T>A	NP_065919.2:p.Val348Asp
XM_017004566.1:c.920T>A	XP_016860055.1:p.Val307Asp
XM_024453023.1:c.1022T>A	XP_024308791.1:p.Val341Asp
XR_923234.2:n.67+1469A>T
NM_001004360.4:c.1022T>A	NP_001004360.3:p.Val341Asp
NM_001178036.2:c.893T>A	NP_001171507.2:p.Val298Asp
NM_001178037.2:c.1031T>A	NP_001171508.2:p.Val344Asp
NM_001321905.2:c.1094T>A	NP_001308834.2:p.Val365Asp
NM_001321907.2:c.1043T>A	NP_001308836.2:p.Val348Asp
NM_001321908.2:c.953T>A	NP_001308837.2:p.Val318Asp
NM_001321909.2:c.926T>A	NP_001308838.2:p.Val309Asp
NM_001321910.2:c.893T>A	NP_001308839.2:p.Val298Asp
NM_001321911.2:c.893T>A	NP_001308840.2:p.Val298Asp
NM_001321912.2:c.893T>A	NP_001308841.2:p.Val298Asp
NM_001321913.2:c.281T>A	NP_001308842.2:p.Val94Asp
NM_020868.6:c.1043T>A MANE Select	NP_065919.3:p.Val348Asp
NM_001004360.5:c.1022T>A	NP_001004360.3:p.Val341Asp
NM_001178036.3:c.893T>A	NP_001171507.2:p.Val298Asp
NM_001178037.3:c.1031T>A	NP_001171508.2:p.Val344Asp
NM_001321905.3:c.1094T>A	NP_001308834.2:p.Val365Asp
NM_001321906.2:c.1022T>A	NP_001308835.2:p.Val341Asp
NM_001321907.3:c.1043T>A	NP_001308836.2:p.Val348Asp
NM_001321908.3:c.953T>A	NP_001308837.2:p.Val318Asp
NM_001321909.3:c.926T>A	NP_001308838.2:p.Val309Asp
NM_001321910.3:c.893T>A	NP_001308839.2:p.Val298Asp
NM_001321911.3:c.893T>A	NP_001308840.2:p.Val298Asp
NM_001321912.3:c.893T>A	NP_001308841.2:p.Val298Asp
NM_001321913.3:c.281T>A	NP_001308842.2:p.Val94Asp
NM_001321914.2:c.281T>A	NP_001308843.2:p.Val94Asp
NM_001399849.1:c.893T>A	NP_001386778.1:p.Val298Asp
NM_001399850.1:c.281T>A	NP_001386779.1:p.Val94Asp
NM_001399851.1:c.791T>A	NP_001386780.1:p.Val264Asp