Canonical Allele Identifier: CA755544364

Gene: DPP10

Linked Data

• dbSNP Id: rs1183012770
• gnomAD v3: 2-115768225-G-GA
• gnomAD v4: 2-115768225-G-GA
• MyVariant Identifiers: chr2:g.116525801_116525802insA (hg19) ; chr2:g.115768225_115768226insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115768227dup , CM000664.2:g.115768227dup	GRCh38
NC_000002.11:g.116525803dup , CM000664.1:g.116525803dup	GRCh37
NC_000002.10:g.116242273dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410059.6:c.1114-70dup MANE Select	ENSP00000386565.1:n.1114-70dup
ENST00000310323.12:c.1093-70dup	ENSP00000309066.8:n.1093-70dup
ENST00000393147.6:c.1126-70dup	ENSP00000376855.2:n.1126-70dup
ENST00000409163.5:c.964-70dup	ENSP00000387038.1:n.964-70dup
ENST00000410059.5:c.1114-70dup	ENSP00000386565.1:n.1114-70dup
NM_001004360.3:c.1093-70dup	NP_001004360.2:n.1093-70dup
NM_001178034.1:c.1126-70dup	NP_001171505.1:n.1126-70dup
NM_001178036.1:c.964-70dup	NP_001171507.1:n.964-70dup
NM_001178037.1:c.1102-70dup	NP_001171508.1:n.1102-70dup
NM_020868.3:c.1114-70dup	NP_065919.2:n.1114-70dup
XM_011511526.1:c.1093-70dup	XP_011509828.1:n.1093-70dup
XM_011511527.1:c.964-70dup	XP_011509829.1:n.964-70dup
XM_011511528.1:c.862-70dup	XP_011509830.1:n.862-70dup
NM_001321905.1:c.1165-70dup	NP_001308834.1:n.1165-70dup
NM_001321906.1:c.1093-70dup	NP_001308835.1:n.1093-70dup
NM_001321907.1:c.1075-70dup	NP_001308836.1:n.1075-70dup
NM_001321908.1:c.1024-70dup	NP_001308837.1:n.1024-70dup
NM_001321909.1:c.997-70dup	NP_001308838.1:n.997-70dup
NM_001321910.1:c.964-70dup	NP_001308839.1:n.964-70dup
NM_001321911.1:c.964-70dup	NP_001308840.1:n.964-70dup
NM_001321912.1:c.964-70dup	NP_001308841.1:n.964-70dup
NM_001321913.1:c.352-70dup	NP_001308842.1:n.352-70dup
NM_001321914.1:c.352-70dup	NP_001308843.1:n.352-70dup
NM_020868.4:c.1114-70dup	NP_065919.2:n.1114-70dup
XM_017004566.1:c.991-70dup	XP_016860055.1:n.991-70dup
XM_024453023.1:c.1054-70dup	XP_024308791.1:n.1054-70dup
NM_001004360.4:c.1093-70dup	NP_001004360.3:n.1093-70dup
NM_001178036.2:c.964-70dup	NP_001171507.2:n.964-70dup
NM_001178037.2:c.1102-70dup	NP_001171508.2:n.1102-70dup
NM_001321905.2:c.1165-70dup	NP_001308834.2:n.1165-70dup
NM_001321907.2:c.1075-70dup	NP_001308836.2:n.1075-70dup
NM_001321908.2:c.1024-70dup	NP_001308837.2:n.1024-70dup
NM_001321909.2:c.997-70dup	NP_001308838.2:n.997-70dup
NM_001321910.2:c.964-70dup	NP_001308839.2:n.964-70dup
NM_001321911.2:c.964-70dup	NP_001308840.2:n.964-70dup
NM_001321912.2:c.964-70dup	NP_001308841.2:n.964-70dup
NM_001321913.2:c.352-70dup	NP_001308842.2:n.352-70dup
NM_020868.6:c.1114-70dup MANE Select	NP_065919.3:n.1114-70dup
NM_001004360.5:c.1093-70dup	NP_001004360.3:n.1093-70dup
NM_001178036.3:c.964-70dup	NP_001171507.2:n.964-70dup
NM_001178037.3:c.1102-70dup	NP_001171508.2:n.1102-70dup
NM_001321905.3:c.1165-70dup	NP_001308834.2:n.1165-70dup
NM_001321906.2:c.1093-70dup	NP_001308835.2:n.1093-70dup
NM_001321907.3:c.1075-70dup	NP_001308836.2:n.1075-70dup
NM_001321908.3:c.1024-70dup	NP_001308837.2:n.1024-70dup
NM_001321909.3:c.997-70dup	NP_001308838.2:n.997-70dup
NM_001321910.3:c.964-70dup	NP_001308839.2:n.964-70dup
NM_001321911.3:c.964-70dup	NP_001308840.2:n.964-70dup
NM_001321912.3:c.964-70dup	NP_001308841.2:n.964-70dup
NM_001321913.3:c.352-70dup	NP_001308842.2:n.352-70dup
NM_001321914.2:c.352-70dup	NP_001308843.2:n.352-70dup
NM_001399849.1:c.964-70dup	NP_001386778.1:n.964-70dup
NM_001399850.1:c.352-70dup	NP_001386779.1:n.352-70dup
NM_001399851.1:c.862-70dup	NP_001386780.1:n.862-70dup