Canonical Allele Identifier: CA2580587697
Gene: APPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.57229366G>T , CM000665.2:g.57229366G>T GRCh38
NC_000003.11:g.57263394G>T , CM000665.1:g.57263394G>T GRCh37
NC_000003.10:g.57238434G>T NCBI36
NG_047003.1:g.6630G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000288266.8:c.54+1429G>T MANE Select ENSP00000288266.3:n.54+1429G>T
ENST00000650354.1:c.54+1429G>T ENSP00000498115.1:n.54+1429G>T
ENST00000288266.7:c.54+1429G>T ENSP00000288266.3:n.54+1429G>T
ENST00000444459.1:c.-51-1348G>T ENSP00000406095.1:n.-51-1348G>T
ENST00000468342.1:n.99+1429G>T
ENST00000482800.5:n.149+1429G>T
ENST00000495803.5:c.54+1429G>T ENSP00000419644.1:n.54+1429G>T
NM_012096.2:c.54+1429G>T NP_036228.1:n.54+1429G>T
XM_011533583.1:c.-51-1348G>T XP_011531885.1:n.-51-1348G>T
XM_011533583.3:c.-51-1348G>T XP_011531885.1:n.-51-1348G>T
NM_012096.3:c.54+1429G>T MANE Select NP_036228.1:n.54+1429G>T