Canonical Allele Identifier: CA1200795713

Gene: PEAR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156899233G= , CM000663.2:g.156899233G=	GRCh38
NC_000001.10:g.156869025G= , CM000663.1:g.156869025G=	GRCh37
NC_000001.9:g.155135649G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000292357.8:c.-9-4685G= MANE Select	ENSP00000292357.7:n.-9-4685G=
ENST00000292357.7:c.-9-4685G=	ENSP00000292357.7:n.-9-4685G=
ENST00000338302.7:c.-107-2955G=	ENSP00000344465.3:n.-107-2955G=
ENST00000444016.5:c.-9-4685G=	ENSP00000397870.1:n.-9-4685G=
ENST00000455314.5:c.-9-4685G=	ENSP00000389742.1:n.-9-4685G=
NM_001080471.1:c.-9-4685G=	NP_001073940.1:n.-9-4685G=
XM_005245141.2:c.-168-2955G=	XP_005245198.1:n.-168-2955G=
XM_006711302.2:c.-168-2955G=	XP_006711365.1:n.-168-2955G=
XM_011509508.1:c.-164-2955G=	XP_011507810.1:n.-164-2955G=
XM_011509509.1:c.-107-2955G=	XP_011507811.1:n.-107-2955G=
XM_011509510.1:c.-107-2955G=	XP_011507812.1:n.-107-2955G=
XM_011509511.1:c.-168-2955G=	XP_011507813.1:n.-168-2955G=
XM_011509512.1:c.-494-4685G=	XP_011507814.1:n.-494-4685G=
NM_001353682.1:c.-347-4685G=	NP_001340611.1:n.-347-4685G=
NM_001353683.1:c.-506-2955G=	NP_001340612.1:n.-506-2955G=
XM_005245141.3:c.-168-2955G=	XP_005245198.1:n.-168-2955G=
XM_011509510.2:c.-107-2955G=	XP_011507812.1:n.-107-2955G=
XM_011509511.2:c.-168-2955G=	XP_011507813.1:n.-168-2955G=
XM_011509512.2:c.-494-4685G=	XP_011507814.1:n.-494-4685G=
XM_017001236.1:c.-70-4624G=	XP_016856725.1:n.-70-4624G=
XM_017001238.1:c.-445-2955G=	XP_016856727.1:n.-445-2955G=
XM_017001239.1:c.-256-4685G=	XP_016856728.1:n.-256-4685G=
XM_017001242.1:c.-69+5396G=	XP_016856731.1:n.-69+5396G=
NM_001353682.2:c.-347-4685G=	NP_001340611.1:n.-347-4685G=
NM_001353683.2:c.-506-2955G=	NP_001340612.1:n.-506-2955G=
NM_001080471.3:c.-9-4685G= MANE Select	NP_001073940.1:n.-9-4685G=