Canonical Allele Identifier: CA348324500

Gene: DPP10

Linked Data

• MyVariant Identifiers: chr2:g.116525951T>G (hg19) ; chr2:g.115768375T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768375T>G , CM000664.2:g.115768375T>G	GRCh38
NC_000002.11:g.116525951T>G , CM000664.1:g.116525951T>G	GRCh37
NC_000002.10:g.116242421T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410059.6:c.1192T>G MANE Select	ENSP00000386565.1:p.Phe398Val
ENST00000310323.12:c.1171T>G	ENSP00000309066.8:p.Phe391Val
ENST00000393147.6:c.1204T>G	ENSP00000376855.2:p.Phe402Val
ENST00000409163.5:c.1042T>G	ENSP00000387038.1:p.Phe348Val
ENST00000410059.5:c.1192T>G	ENSP00000386565.1:p.Phe398Val
NM_001004360.3:c.1171T>G	NP_001004360.2:p.Phe391Val
NM_001178034.1:c.1204T>G	NP_001171505.1:p.Phe402Val
NM_001178036.1:c.1042T>G	NP_001171507.1:p.Phe348Val
NM_001178037.1:c.1180T>G	NP_001171508.1:p.Phe394Val
NM_020868.3:c.1192T>G	NP_065919.2:p.Phe398Val
XM_011511526.1:c.1171T>G	XP_011509828.1:p.Phe391Val
XM_011511527.1:c.1042T>G	XP_011509829.1:p.Phe348Val
XM_011511528.1:c.940T>G	XP_011509830.1:p.Phe314Val
NM_001321905.1:c.1243T>G	NP_001308834.1:p.Phe415Val
NM_001321906.1:c.1171T>G	NP_001308835.1:p.Phe391Val
NM_001321907.1:c.1153T>G	NP_001308836.1:p.Phe385Val
NM_001321908.1:c.1102T>G	NP_001308837.1:p.Phe368Val
NM_001321909.1:c.1075T>G	NP_001308838.1:p.Phe359Val
NM_001321910.1:c.1042T>G	NP_001308839.1:p.Phe348Val
NM_001321911.1:c.1042T>G	NP_001308840.1:p.Phe348Val
NM_001321912.1:c.1042T>G	NP_001308841.1:p.Phe348Val
NM_001321913.1:c.430T>G	NP_001308842.1:p.Phe144Val
NM_001321914.1:c.430T>G	NP_001308843.1:p.Phe144Val
NM_020868.4:c.1192T>G	NP_065919.2:p.Phe398Val
XM_017004566.1:c.1069T>G	XP_016860055.1:p.Phe357Val
XM_024453023.1:c.1132T>G	XP_024308791.1:p.Phe378Val
NM_001004360.4:c.1171T>G	NP_001004360.3:p.Phe391Val
NM_001178036.2:c.1042T>G	NP_001171507.2:p.Phe348Val
NM_001178037.2:c.1180T>G	NP_001171508.2:p.Phe394Val
NM_001321905.2:c.1243T>G	NP_001308834.2:p.Phe415Val
NM_001321907.2:c.1153T>G	NP_001308836.2:p.Phe385Val
NM_001321908.2:c.1102T>G	NP_001308837.2:p.Phe368Val
NM_001321909.2:c.1075T>G	NP_001308838.2:p.Phe359Val
NM_001321910.2:c.1042T>G	NP_001308839.2:p.Phe348Val
NM_001321911.2:c.1042T>G	NP_001308840.2:p.Phe348Val
NM_001321912.2:c.1042T>G	NP_001308841.2:p.Phe348Val
NM_001321913.2:c.430T>G	NP_001308842.2:p.Phe144Val
NM_020868.6:c.1192T>G MANE Select	NP_065919.3:p.Phe398Val
NM_001004360.5:c.1171T>G	NP_001004360.3:p.Phe391Val
NM_001178036.3:c.1042T>G	NP_001171507.2:p.Phe348Val
NM_001178037.3:c.1180T>G	NP_001171508.2:p.Phe394Val
NM_001321905.3:c.1243T>G	NP_001308834.2:p.Phe415Val
NM_001321906.2:c.1171T>G	NP_001308835.2:p.Phe391Val
NM_001321907.3:c.1153T>G	NP_001308836.2:p.Phe385Val
NM_001321908.3:c.1102T>G	NP_001308837.2:p.Phe368Val
NM_001321909.3:c.1075T>G	NP_001308838.2:p.Phe359Val
NM_001321910.3:c.1042T>G	NP_001308839.2:p.Phe348Val
NM_001321911.3:c.1042T>G	NP_001308840.2:p.Phe348Val
NM_001321912.3:c.1042T>G	NP_001308841.2:p.Phe348Val
NM_001321913.3:c.430T>G	NP_001308842.2:p.Phe144Val
NM_001321914.2:c.430T>G	NP_001308843.2:p.Phe144Val
NM_001399849.1:c.1042T>G	NP_001386778.1:p.Phe348Val
NM_001399850.1:c.430T>G	NP_001386779.1:p.Phe144Val
NM_001399851.1:c.940T>G	NP_001386780.1:p.Phe314Val