Canonical Allele Identifier: CA1048310832

Gene: APPL1

Linked Data

• dbSNP Id: rs2060672406
• gnomAD v3: 3-57229328-T-G
• gnomAD v4: 3-57229328-T-G

Genomic Alleles

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

Transcript Alleles

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