Canonical Allele Identifier: CA2660827064

Gene: DPP10

Linked Data

• gnomAD v4: 2-115768284-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768284T>C , CM000664.2:g.115768284T>C	GRCh38
NC_000002.11:g.116525860T>C , CM000664.1:g.116525860T>C	GRCh37
NC_000002.10:g.116242330T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410059.6:c.1114-13T>C MANE Select	ENSP00000386565.1:n.1114-13T>C
ENST00000310323.12:c.1093-13T>C	ENSP00000309066.8:n.1093-13T>C
ENST00000393147.6:c.1126-13T>C	ENSP00000376855.2:n.1126-13T>C
ENST00000409163.5:c.964-13T>C	ENSP00000387038.1:n.964-13T>C
ENST00000410059.5:c.1114-13T>C	ENSP00000386565.1:n.1114-13T>C
NM_001004360.3:c.1093-13T>C	NP_001004360.2:n.1093-13T>C
NM_001178034.1:c.1126-13T>C	NP_001171505.1:n.1126-13T>C
NM_001178036.1:c.964-13T>C	NP_001171507.1:n.964-13T>C
NM_001178037.1:c.1102-13T>C	NP_001171508.1:n.1102-13T>C
NM_020868.3:c.1114-13T>C	NP_065919.2:n.1114-13T>C
XM_011511526.1:c.1093-13T>C	XP_011509828.1:n.1093-13T>C
XM_011511527.1:c.964-13T>C	XP_011509829.1:n.964-13T>C
XM_011511528.1:c.862-13T>C	XP_011509830.1:n.862-13T>C
NM_001321905.1:c.1165-13T>C	NP_001308834.1:n.1165-13T>C
NM_001321906.1:c.1093-13T>C	NP_001308835.1:n.1093-13T>C
NM_001321907.1:c.1075-13T>C	NP_001308836.1:n.1075-13T>C
NM_001321908.1:c.1024-13T>C	NP_001308837.1:n.1024-13T>C
NM_001321909.1:c.997-13T>C	NP_001308838.1:n.997-13T>C
NM_001321910.1:c.964-13T>C	NP_001308839.1:n.964-13T>C
NM_001321911.1:c.964-13T>C	NP_001308840.1:n.964-13T>C
NM_001321912.1:c.964-13T>C	NP_001308841.1:n.964-13T>C
NM_001321913.1:c.352-13T>C	NP_001308842.1:n.352-13T>C
NM_001321914.1:c.352-13T>C	NP_001308843.1:n.352-13T>C
NM_020868.4:c.1114-13T>C	NP_065919.2:n.1114-13T>C
XM_017004566.1:c.991-13T>C	XP_016860055.1:n.991-13T>C
XM_024453023.1:c.1054-13T>C	XP_024308791.1:n.1054-13T>C
NM_001004360.4:c.1093-13T>C	NP_001004360.3:n.1093-13T>C
NM_001178036.2:c.964-13T>C	NP_001171507.2:n.964-13T>C
NM_001178037.2:c.1102-13T>C	NP_001171508.2:n.1102-13T>C
NM_001321905.2:c.1165-13T>C	NP_001308834.2:n.1165-13T>C
NM_001321907.2:c.1075-13T>C	NP_001308836.2:n.1075-13T>C
NM_001321908.2:c.1024-13T>C	NP_001308837.2:n.1024-13T>C
NM_001321909.2:c.997-13T>C	NP_001308838.2:n.997-13T>C
NM_001321910.2:c.964-13T>C	NP_001308839.2:n.964-13T>C
NM_001321911.2:c.964-13T>C	NP_001308840.2:n.964-13T>C
NM_001321912.2:c.964-13T>C	NP_001308841.2:n.964-13T>C
NM_001321913.2:c.352-13T>C	NP_001308842.2:n.352-13T>C
NM_020868.6:c.1114-13T>C MANE Select	NP_065919.3:n.1114-13T>C
NM_001004360.5:c.1093-13T>C	NP_001004360.3:n.1093-13T>C
NM_001178036.3:c.964-13T>C	NP_001171507.2:n.964-13T>C
NM_001178037.3:c.1102-13T>C	NP_001171508.2:n.1102-13T>C
NM_001321905.3:c.1165-13T>C	NP_001308834.2:n.1165-13T>C
NM_001321906.2:c.1093-13T>C	NP_001308835.2:n.1093-13T>C
NM_001321907.3:c.1075-13T>C	NP_001308836.2:n.1075-13T>C
NM_001321908.3:c.1024-13T>C	NP_001308837.2:n.1024-13T>C
NM_001321909.3:c.997-13T>C	NP_001308838.2:n.997-13T>C
NM_001321910.3:c.964-13T>C	NP_001308839.2:n.964-13T>C
NM_001321911.3:c.964-13T>C	NP_001308840.2:n.964-13T>C
NM_001321912.3:c.964-13T>C	NP_001308841.2:n.964-13T>C
NM_001321913.3:c.352-13T>C	NP_001308842.2:n.352-13T>C
NM_001321914.2:c.352-13T>C	NP_001308843.2:n.352-13T>C
NM_001399849.1:c.964-13T>C	NP_001386778.1:n.964-13T>C
NM_001399850.1:c.352-13T>C	NP_001386779.1:n.352-13T>C
NM_001399851.1:c.862-13T>C	NP_001386780.1:n.862-13T>C