Canonical Allele Identifier: CA1367098253

Gene: APPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57229328T= , CM000665.2:g.57229328T=	GRCh38
NC_000003.11:g.57263356T= , CM000665.1:g.57263356T=	GRCh37
NC_000003.10:g.57238396T=	NCBI36
NG_047003.1:g.6592T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288266.8:c.54+1391T= MANE Select	ENSP00000288266.3:n.54+1391T=
ENST00000650354.1:c.54+1391T=	ENSP00000498115.1:n.54+1391T=
ENST00000288266.7:c.54+1391T=	ENSP00000288266.3:n.54+1391T=
ENST00000444459.1:c.-51-1386T=	ENSP00000406095.1:n.-51-1386T=
ENST00000468342.1:n.99+1391T=
ENST00000482800.5:n.149+1391T=
ENST00000495803.5:c.54+1391T=	ENSP00000419644.1:n.54+1391T=
NM_012096.2:c.54+1391T=	NP_036228.1:n.54+1391T=
XM_011533583.1:c.-51-1386T=	XP_011531885.1:n.-51-1386T=
XM_011533583.3:c.-51-1386T=	XP_011531885.1:n.-51-1386T=
NM_012096.3:c.54+1391T= MANE Select	NP_036228.1:n.54+1391T=