Canonical Allele Identifier: CA1367098247
Gene: APPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.57229320A= , CM000665.2:g.57229320A= GRCh38
NC_000003.11:g.57263348A= , CM000665.1:g.57263348A= GRCh37
NC_000003.10:g.57238388A= NCBI36
NG_047003.1:g.6584A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288266.8:c.54+1383A= MANE Select ENSP00000288266.3:n.54+1383A=
ENST00000650354.1:c.54+1383A= ENSP00000498115.1:n.54+1383A=
ENST00000288266.7:c.54+1383A= ENSP00000288266.3:n.54+1383A=
ENST00000444459.1:c.-52+1383A= ENSP00000406095.1:n.-52+1383A=
ENST00000468342.1:n.99+1383A=
ENST00000482800.5:n.149+1383A=
ENST00000495803.5:c.54+1383A= ENSP00000419644.1:n.54+1383A=
NM_012096.2:c.54+1383A= NP_036228.1:n.54+1383A=
XM_011533583.1:c.-52+1383A= XP_011531885.1:n.-52+1383A=
XM_011533583.3:c.-52+1383A= XP_011531885.1:n.-52+1383A=
NM_012096.3:c.54+1383A= MANE Select NP_036228.1:n.54+1383A=