Canonical Allele Identifier: CA1367098324
Gene: APPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.57229454G= , CM000665.2:g.57229454G= GRCh38
NC_000003.11:g.57263482G= , CM000665.1:g.57263482G= GRCh37
NC_000003.10:g.57238522G= NCBI36
NG_047003.1:g.6718G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288266.8:c.54+1517G= MANE Select ENSP00000288266.3:n.54+1517G=
ENST00000650354.1:c.54+1517G= ENSP00000498115.1:n.54+1517G=
ENST00000288266.7:c.54+1517G= ENSP00000288266.3:n.54+1517G=
ENST00000444459.1:c.-51-1260G= ENSP00000406095.1:n.-51-1260G=
ENST00000468342.1:n.99+1517G=
ENST00000482800.5:n.149+1517G=
ENST00000495803.5:c.54+1517G= ENSP00000419644.1:n.54+1517G=
NM_012096.2:c.54+1517G= NP_036228.1:n.54+1517G=
XM_011533583.1:c.-51-1260G= XP_011531885.1:n.-51-1260G=
XM_011533583.3:c.-51-1260G= XP_011531885.1:n.-51-1260G=
NM_012096.3:c.54+1517G= MANE Select NP_036228.1:n.54+1517G=