Canonical Allele Identifier: CA2060497528
Gene: APPL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105189791T= , CM000674.2:g.105189791T= GRCh38
NC_000012.11:g.105583569T= , CM000674.1:g.105583569T= GRCh37
NC_000012.10:g.104107699T= NCBI36
NG_030419.1:g.51440A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258530.8:c.1440A= MANE Select ENSP00000258530.3:p.Glu480=
ENST00000258530.7:c.1440A= ENSP00000258530.3:p.Glu480=
ENST00000539978.6:c.1311A= ENSP00000444472.2:p.Glu437=
ENST00000547439.5:c.*725A= ENSP00000449410.1:n.*725A=
ENST00000547809.5:n.1450A=
ENST00000551662.5:c.1458A= ENSP00000446917.1:p.Glu486=
ENST00000552945.1:n.280A=
ENST00000553109.1:c.84A= ENSP00000446510.1:p.Glu28=
NM_001251904.1:c.1458A= NP_001238833.1:p.Glu486=
NM_001251905.1:c.1311A= NP_001238834.1:p.Glu437=
NM_018171.3:c.1440A= NP_060641.2:p.Glu480=
XM_006719472.1:c.1458A= XP_006719535.1:p.Glu486=
XM_011538530.1:c.1419A= XP_011536832.1:p.Glu473=
XM_011538531.1:c.1329A= XP_011536833.1:p.Glu443=
XM_011538532.1:c.1329A= XP_011536834.1:p.Glu443=
XM_011538530.3:c.1419A= XP_011536832.1:p.Glu473=
XM_011538531.3:c.1329A= XP_011536833.1:p.Glu443=
XM_011538532.3:c.1329A= XP_011536834.1:p.Glu443=
XM_017019551.2:c.1401A= XP_016875040.1:p.Glu467=
XM_017019552.2:c.1311A= XP_016875041.1:p.Glu437=
XM_017019553.2:c.1311A= XP_016875042.1:p.Glu437=
XM_017019554.1:c.1440A= XP_016875043.1:p.Glu480=
XR_001748795.1:n.1620A=
XR_001748796.1:n.1602A=
NM_018171.4:c.1440A= NP_060641.2:p.Glu480=
NM_018171.5:c.1440A= MANE Select NP_060641.2:p.Glu480=
NM_001251904.2:c.1458A= NP_001238833.1:p.Glu486=
NM_001251905.2:c.1311A= NP_001238834.1:p.Glu437=