Canonical Allele Identifier: CA2060497389

Gene: APPL2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105189489_105189505delinsGCATTTGAATGTGATAA , CM000674.2:g.105189489_105189505delinsGCATTTGAATGTGATAA	GRCh38
NC_000012.11:g.105583267_105583283delinsGCATTTGAATGTGATAA , CM000674.1:g.105583267_105583283delinsGCATTTGAATGTGATAA	GRCh37
NC_000012.10:g.104107397_104107413delinsGCATTTGAATGTGATAA	NCBI36
NG_030419.1:g.51726_51742delinsTTATCACATTCAAATGC

Transcript Alleles

HGVS	Amino-acid Change
NM_018171.5:c.1459+267_1459+283delinsTTATCACATTCAAATGC MANE Select	NP_060641.2:n.1459+267_1459+283delinsTTATCACATTCAAATGC
ENST00000258530.8:c.1459+267_1459+283delinsTTATCACATTCAAATGC MANE Select	ENSP00000258530.3:n.1459+267_1459+283delinsTTATCACATTCAAATGC
NM_001251904.1:c.1477+267_1477+283delinsTTATCACATTCAAATGC	NP_001238833.1:n.1477+267_1477+283delinsTTATCACATTCAAATGC
NM_001251904.2:c.1477+267_1477+283delinsTTATCACATTCAAATGC	NP_001238833.1:n.1477+267_1477+283delinsTTATCACATTCAAATGC
NM_001251905.1:c.1330+267_1330+283delinsTTATCACATTCAAATGC	NP_001238834.1:n.1330+267_1330+283delinsTTATCACATTCAAATGC
NM_001251905.2:c.1330+267_1330+283delinsTTATCACATTCAAATGC	NP_001238834.1:n.1330+267_1330+283delinsTTATCACATTCAAATGC
NM_018171.3:c.1459+267_1459+283delinsTTATCACATTCAAATGC	NP_060641.2:n.1459+267_1459+283delinsTTATCACATTCAAATGC
NM_018171.4:c.1459+267_1459+283delinsTTATCACATTCAAATGC	NP_060641.2:n.1459+267_1459+283delinsTTATCACATTCAAATGC
ENST00000258530.7:c.1459+267_1459+283delinsTTATCACATTCAAATGC	ENSP00000258530.3:n.1459+267_1459+283delinsTTATCACATTCAAATGC
ENST00000539978.6:c.1330+267_1330+283delinsTTATCACATTCAAATGC	ENSP00000444472.2:n.1330+267_1330+283delinsTTATCACATTCAAATGC
ENST00000547439.5:c.*744+267_*744+283delinsTTATCACATTCAAATGC	ENSP00000449410.1:n.*744+267_*744+283delinsTTATCACATTCAAATGC
ENST00000547809.5:n.1469+267_1469+283delinsTTATCACATTCAAATGC
ENST00000551662.5:c.1477+267_1477+283delinsTTATCACATTCAAATGC	ENSP00000446917.1:n.1477+267_1477+283delinsTTATCACATTCAAATGC
ENST00000552945.1:n.299+267_299+283delinsTTATCACATTCAAATGC
ENST00000553109.1:c.103+267_103+283delinsTTATCACATTCAAATGC	ENSP00000446510.1:n.103+267_103+283delinsTTATCACATTCAAATGC
XM_006719472.1:c.1477+267_1477+283delinsTTATCACATTCAAATGC	XP_006719535.1:n.1477+267_1477+283delinsTTATCACATTCAAATGC
XM_011538530.1:c.1438+267_1438+283delinsTTATCACATTCAAATGC	XP_011536832.1:n.1438+267_1438+283delinsTTATCACATTCAAATGC
XM_011538530.3:c.1438+267_1438+283delinsTTATCACATTCAAATGC	XP_011536832.1:n.1438+267_1438+283delinsTTATCACATTCAAATGC
XM_011538531.1:c.1348+267_1348+283delinsTTATCACATTCAAATGC	XP_011536833.1:n.1348+267_1348+283delinsTTATCACATTCAAATGC
XM_011538531.3:c.1348+267_1348+283delinsTTATCACATTCAAATGC	XP_011536833.1:n.1348+267_1348+283delinsTTATCACATTCAAATGC
XM_011538532.1:c.1348+267_1348+283delinsTTATCACATTCAAATGC	XP_011536834.1:n.1348+267_1348+283delinsTTATCACATTCAAATGC
XM_011538532.3:c.1348+267_1348+283delinsTTATCACATTCAAATGC	XP_011536834.1:n.1348+267_1348+283delinsTTATCACATTCAAATGC
XM_017019551.2:c.1420+267_1420+283delinsTTATCACATTCAAATGC	XP_016875040.1:n.1420+267_1420+283delinsTTATCACATTCAAATGC
XM_017019552.2:c.1330+267_1330+283delinsTTATCACATTCAAATGC	XP_016875041.1:n.1330+267_1330+283delinsTTATCACATTCAAATGC
XM_017019553.2:c.1330+267_1330+283delinsTTATCACATTCAAATGC	XP_016875042.1:n.1330+267_1330+283delinsTTATCACATTCAAATGC
XM_017019554.1:c.1459+267_1459+283delinsTTATCACATTCAAATGC	XP_016875043.1:n.1459+267_1459+283delinsTTATCACATTCAAATGC
XR_001748795.1:n.1639+267_1639+283delinsTTATCACATTCAAATGC
XR_001748796.1:n.1621+267_1621+283delinsTTATCACATTCAAATGC