Canonical Allele Identifier: CA2060497507
Gene: APPL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105189746A= , CM000674.2:g.105189746A= GRCh38
NC_000012.11:g.105583524A= , CM000674.1:g.105583524A= GRCh37
NC_000012.10:g.104107654A= NCBI36
NG_030419.1:g.51485T=

Transcript Alleles

HGVS Amino-acid change
ENST00000258530.8:c.1459+26T= MANE Select ENSP00000258530.3:n.1459+26T=
ENST00000258530.7:c.1459+26T= ENSP00000258530.3:n.1459+26T=
ENST00000539978.6:c.1330+26T= ENSP00000444472.2:n.1330+26T=
ENST00000547439.5:c.*744+26T= ENSP00000449410.1:n.*744+26T=
ENST00000547809.5:n.1469+26T=
ENST00000551662.5:c.1477+26T= ENSP00000446917.1:n.1477+26T=
ENST00000552945.1:n.299+26T=
ENST00000553109.1:n.103+26T= ENSP00000446510.1:n.103+26T=
NM_001251904.1:c.1477+26T= NP_001238833.1:n.1477+26T=
NM_001251905.1:c.1330+26T= NP_001238834.1:n.1330+26T=
NM_018171.3:c.1459+26T= NP_060641.2:n.1459+26T=
XM_006719472.1:c.1477+26T= XP_006719535.1:n.1477+26T=
XM_011538530.1:c.1438+26T= XP_011536832.1:n.1438+26T=
XM_011538531.1:c.1348+26T= XP_011536833.1:n.1348+26T=
XM_011538532.1:c.1348+26T= XP_011536834.1:n.1348+26T=
XM_011538530.3:c.1438+26T= XP_011536832.1:n.1438+26T=
XM_011538531.3:c.1348+26T= XP_011536833.1:n.1348+26T=
XM_011538532.3:c.1348+26T= XP_011536834.1:n.1348+26T=
XM_017019551.2:c.1420+26T= XP_016875040.1:n.1420+26T=
XM_017019552.2:c.1330+26T= XP_016875041.1:n.1330+26T=
XM_017019553.2:c.1330+26T= XP_016875042.1:n.1330+26T=
XM_017019554.1:c.1459+26T= XP_016875043.1:n.1459+26T=
XR_001748795.1:n.1639+26T=
XR_001748796.1:n.1621+26T=
NM_018171.4:c.1459+26T= NP_060641.2:n.1459+26T=
NM_018171.5:c.1459+26T= MANE Select NP_060641.2:n.1459+26T=
NM_001251904.2:c.1477+26T= NP_001238833.1:n.1477+26T=
NM_001251905.2:c.1330+26T= NP_001238834.1:n.1330+26T=