Canonical Allele Identifier: CA1281303688

Gene: DPP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115733716A= , CM000664.2:g.115733716A=	GRCh38
NC_000002.11:g.116491292A= , CM000664.1:g.116491292A=	GRCh37
NC_000002.10:g.116207762A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410059.6:c.697+5780A= MANE Select	ENSP00000386565.1:n.697+5780A=
ENST00000310323.12:c.676+5780A=	ENSP00000309066.8:n.676+5780A=
ENST00000393146.6:c.685+5780A=	ENSP00000376854.2:n.685+5780A=
ENST00000393147.6:c.709+5780A=	ENSP00000376855.2:n.709+5780A=
ENST00000409163.5:c.547+5780A=	ENSP00000387038.1:n.547+5780A=
ENST00000410059.5:c.697+5780A=	ENSP00000386565.1:n.697+5780A=
ENST00000488208.1:n.519+5780A=
NM_001004360.3:c.676+5780A=	NP_001004360.2:n.676+5780A=
NM_001178034.1:c.709+5780A=	NP_001171505.1:n.709+5780A=
NM_001178036.1:c.547+5780A=	NP_001171507.1:n.547+5780A=
NM_001178037.1:c.685+5780A=	NP_001171508.1:n.685+5780A=
NM_020868.3:c.697+5780A=	NP_065919.2:n.697+5780A=
XM_011511526.1:c.676+5780A=	XP_011509828.1:n.676+5780A=
XM_011511527.1:c.547+5780A=	XP_011509829.1:n.547+5780A=
XM_011511528.1:c.445+5780A=	XP_011509830.1:n.445+5780A=
NM_001321905.1:c.748+5780A=	NP_001308834.1:n.748+5780A=
NM_001321906.1:c.676+5780A=	NP_001308835.1:n.676+5780A=
NM_001321907.1:c.697+5780A=	NP_001308836.1:n.697+5780A=
NM_001321908.1:c.607+5780A=	NP_001308837.1:n.607+5780A=
NM_001321909.1:c.580+5780A=	NP_001308838.1:n.580+5780A=
NM_001321910.1:c.547+5780A=	NP_001308839.1:n.547+5780A=
NM_001321911.1:c.547+5780A=	NP_001308840.1:n.547+5780A=
NM_001321912.1:c.547+5780A=	NP_001308841.1:n.547+5780A=
NM_001321913.1:c.-66+5780A=	NP_001308842.1:n.-66+5780A=
NM_001321914.1:c.-66+5780A=	NP_001308843.1:n.-66+5780A=
NM_020868.4:c.697+5780A=	NP_065919.2:n.697+5780A=
XM_017004566.1:c.574+5780A=	XP_016860055.1:n.574+5780A=
XM_024453023.1:c.676+5780A=	XP_024308791.1:n.676+5780A=
NM_001004360.4:c.676+5780A=	NP_001004360.3:n.676+5780A=
NM_001178036.2:c.547+5780A=	NP_001171507.2:n.547+5780A=
NM_001178037.2:c.685+5780A=	NP_001171508.2:n.685+5780A=
NM_001321905.2:c.748+5780A=	NP_001308834.2:n.748+5780A=
NM_001321907.2:c.697+5780A=	NP_001308836.2:n.697+5780A=
NM_001321908.2:c.607+5780A=	NP_001308837.2:n.607+5780A=
NM_001321909.2:c.580+5780A=	NP_001308838.2:n.580+5780A=
NM_001321910.2:c.547+5780A=	NP_001308839.2:n.547+5780A=
NM_001321911.2:c.547+5780A=	NP_001308840.2:n.547+5780A=
NM_001321912.2:c.547+5780A=	NP_001308841.2:n.547+5780A=
NM_001321913.2:c.-66+5780A=	NP_001308842.2:n.-66+5780A=
NM_020868.6:c.697+5780A= MANE Select	NP_065919.3:n.697+5780A=
NM_001004360.5:c.676+5780A=	NP_001004360.3:n.676+5780A=
NM_001178036.3:c.547+5780A=	NP_001171507.2:n.547+5780A=
NM_001178037.3:c.685+5780A=	NP_001171508.2:n.685+5780A=
NM_001321905.3:c.748+5780A=	NP_001308834.2:n.748+5780A=
NM_001321906.2:c.676+5780A=	NP_001308835.2:n.676+5780A=
NM_001321907.3:c.697+5780A=	NP_001308836.2:n.697+5780A=
NM_001321908.3:c.607+5780A=	NP_001308837.2:n.607+5780A=
NM_001321909.3:c.580+5780A=	NP_001308838.2:n.580+5780A=
NM_001321910.3:c.547+5780A=	NP_001308839.2:n.547+5780A=
NM_001321911.3:c.547+5780A=	NP_001308840.2:n.547+5780A=
NM_001321912.3:c.547+5780A=	NP_001308841.2:n.547+5780A=
NM_001321913.3:c.-66+5780A=	NP_001308842.2:n.-66+5780A=
NM_001321914.2:c.-66+5780A=	NP_001308843.2:n.-66+5780A=
NM_001399849.1:c.547+5780A=	NP_001386778.1:n.547+5780A=
NM_001399850.1:c.-96+5780A=	NP_001386779.1:n.-96+5780A=
NM_001399851.1:c.445+5780A=	NP_001386780.1:n.445+5780A=