Canonical Allele Identifier: CA1048310849
Gene: APPL1 HGNC NCBI

Linked Data

gnomAD v3: 3-57229341-G-T
gnomAD v4: 3-57229341-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.57229341G>T , CM000665.2:g.57229341G>T GRCh38
NC_000003.11:g.57263369G>T , CM000665.1:g.57263369G>T GRCh37
NC_000003.10:g.57238409G>T NCBI36
NG_047003.1:g.6605G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000288266.8:c.54+1404G>T MANE Select ENSP00000288266.3:n.54+1404G>T
ENST00000650354.1:c.54+1404G>T ENSP00000498115.1:n.54+1404G>T
ENST00000288266.7:c.54+1404G>T ENSP00000288266.3:n.54+1404G>T
ENST00000444459.1:c.-51-1373G>T ENSP00000406095.1:n.-51-1373G>T
ENST00000468342.1:n.99+1404G>T
ENST00000482800.5:n.149+1404G>T
ENST00000495803.5:c.54+1404G>T ENSP00000419644.1:n.54+1404G>T
NM_012096.2:c.54+1404G>T NP_036228.1:n.54+1404G>T
XM_011533583.1:c.-51-1373G>T XP_011531885.1:n.-51-1373G>T
XM_011533583.3:c.-51-1373G>T XP_011531885.1:n.-51-1373G>T
NM_012096.3:c.54+1404G>T MANE Select NP_036228.1:n.54+1404G>T