Canonical Allele Identifier: CA1200795726

Gene: PEAR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156899267_156899269delinsTGA , CM000663.2:g.156899267_156899269delinsTGA	GRCh38
NC_000001.10:g.156869059_156869061delinsTGA , CM000663.1:g.156869059_156869061delinsTGA	GRCh37
NC_000001.9:g.155135683_155135685delinsTGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292357.8:c.-9-4651_-9-4649delinsTGA MANE Select	ENSP00000292357.7:n.-9-4651_-9-4649delinsTGA
ENST00000292357.7:c.-9-4651_-9-4649delinsTGA	ENSP00000292357.7:n.-9-4651_-9-4649delinsTGA
ENST00000338302.7:c.-107-2921_-107-2919delinsTGA	ENSP00000344465.3:n.-107-2921_-107-2919delinsTGA
ENST00000444016.5:c.-9-4651_-9-4649delinsTGA	ENSP00000397870.1:n.-9-4651_-9-4649delinsTGA
ENST00000455314.5:c.-9-4651_-9-4649delinsTGA	ENSP00000389742.1:n.-9-4651_-9-4649delinsTGA
NM_001080471.1:c.-9-4651_-9-4649delinsTGA	NP_001073940.1:n.-9-4651_-9-4649delinsTGA
XM_005245141.2:c.-168-2921_-168-2919delinsTGA	XP_005245198.1:n.-168-2921_-168-2919delinsTGA
XM_006711302.2:c.-168-2921_-168-2919delinsTGA	XP_006711365.1:n.-168-2921_-168-2919delinsTGA
XM_011509508.1:c.-164-2921_-164-2919delinsTGA	XP_011507810.1:n.-164-2921_-164-2919delinsTGA
XM_011509509.1:c.-107-2921_-107-2919delinsTGA	XP_011507811.1:n.-107-2921_-107-2919delinsTGA
XM_011509510.1:c.-107-2921_-107-2919delinsTGA	XP_011507812.1:n.-107-2921_-107-2919delinsTGA
XM_011509511.1:c.-168-2921_-168-2919delinsTGA	XP_011507813.1:n.-168-2921_-168-2919delinsTGA
XM_011509512.1:c.-494-4651_-494-4649delinsTGA	XP_011507814.1:n.-494-4651_-494-4649delinsTGA
NM_001353682.1:c.-347-4651_-347-4649delinsTGA	NP_001340611.1:n.-347-4651_-347-4649delinsTGA
NM_001353683.1:c.-506-2921_-506-2919delinsTGA	NP_001340612.1:n.-506-2921_-506-2919delinsTGA
XM_005245141.3:c.-168-2921_-168-2919delinsTGA	XP_005245198.1:n.-168-2921_-168-2919delinsTGA
XM_011509510.2:c.-107-2921_-107-2919delinsTGA	XP_011507812.1:n.-107-2921_-107-2919delinsTGA
XM_011509511.2:c.-168-2921_-168-2919delinsTGA	XP_011507813.1:n.-168-2921_-168-2919delinsTGA
XM_011509512.2:c.-494-4651_-494-4649delinsTGA	XP_011507814.1:n.-494-4651_-494-4649delinsTGA
XM_017001236.1:c.-70-4590_-70-4588delinsTGA	XP_016856725.1:n.-70-4590_-70-4588delinsTGA
XM_017001238.1:c.-445-2921_-445-2919delinsTGA	XP_016856727.1:n.-445-2921_-445-2919delinsTGA
XM_017001239.1:c.-256-4651_-256-4649delinsTGA	XP_016856728.1:n.-256-4651_-256-4649delinsTGA
XM_017001242.1:c.-69+5430_-69+5432delinsTGA	XP_016856731.1:n.-69+5430_-69+5432delinsTGA
NM_001353682.2:c.-347-4651_-347-4649delinsTGA	NP_001340611.1:n.-347-4651_-347-4649delinsTGA
NM_001353683.2:c.-506-2921_-506-2919delinsTGA	NP_001340612.1:n.-506-2921_-506-2919delinsTGA
NM_001080471.3:c.-9-4651_-9-4649delinsTGA MANE Select	NP_001073940.1:n.-9-4651_-9-4649delinsTGA