Canonical Allele Identifier: CA1189946033
Gene: AP4B1 HGNC NCBI
AP4B1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113896245C= , CM000663.2:g.113896245C= GRCh38
NC_000001.10:g.114438867C= , CM000663.1:g.114438867C= GRCh37
NC_000001.9:g.114240390C= NCBI36
NG_031901.1:g.13875G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369564.6:c.1285+13G= (AP4B1) ENSP00000358577.2:n.1285+13G=
ENST00000369567.6:c.1006+13G= (AP4B1) ENSP00000358580.1:n.1006+13G=
ENST00000369571.3:c.1510+13G= (AP4B1) ENSP00000358584.3:n.1510+13G=
ENST00000432415.6:c.1006+13G= (AP4B1) ENSP00000393622.2:n.1006+13G=
ENST00000460653.2:c.*580+13G= (AP4B1) ENSP00000518881.1:n.*580+13G=
ENST00000484201.6:c.*260+13G= (AP4B1) ENSP00000518883.1:n.*260+13G=
ENST00000489499.6:c.*852+13G= (AP4B1) ENSP00000518882.1:n.*852+13G=
ENST00000713588.1:c.*621+13G= (AP4B1) ENSP00000518880.1:n.*621+13G=
ENST00000713590.1:c.1510+13G= (AP4B1) ENSP00000518886.1:n.1510+13G=
ENST00000369569.6:c.1510+13G= (AP4B1) MANE Select ENSP00000358582.1:n.1510+13G=
ENST00000256658.8:c.1510+13G= (AP4B1) ENSP00000256658.4:n.1510+13G=
ENST00000369567.5:c.1006+13G= (AP4B1) ENSP00000358580.1:n.1006+13G=
ENST00000369569.5:c.1510+13G= (AP4B1) ENSP00000358582.1:n.1510+13G=
ENST00000462591.1:n.1682+13G= (AP4B1)
ENST00000479285.5:n.751G= (AP4B1)
ENST00000479801.1:n.357G= (AP4B1)
NM_001253852.1:c.1510+13G= (AP4B1) NP_001240781.1:n.1510+13G=
NM_001253852.2:c.1510+13G= (AP4B1) NP_001240781.1:n.1510+13G=
NM_001253853.1:c.1213+13G= (AP4B1) NP_001240782.1:n.1213+13G=
NM_001253853.2:c.1213+13G= (AP4B1) NP_001240782.1:n.1213+13G=
NM_001308312.1:c.1006+13G= (AP4B1) NP_001295241.1:n.1006+13G=
NM_006594.3:c.1510+13G= (AP4B1) NP_006585.2:n.1510+13G=
NM_006594.4:c.1510+13G= (AP4B1) NP_006585.2:n.1510+13G=
NR_037864.1:n.247-1623C= (AP4B1-AS1)
NR_125965.1:n.415-1623C= (AP4B1-AS1)
XM_005270381.2:c.1199-207G= (AP4B1) XP_005270438.1:n.1199-207G=
XM_011540523.1:c.1285+13G= (AP4B1) XP_011538825.1:n.1285+13G=
XM_011540524.1:c.1285+13G= (AP4B1) XP_011538826.1:n.1285+13G=
XM_011540525.1:c.1231+13G= (AP4B1) XP_011538827.1:n.1231+13G=
XM_011540527.1:c.892+13G= (AP4B1) XP_011538829.1:n.892+13G=
XM_011540528.1:c.535+13G= (AP4B1) XP_011538830.1:n.535+13G=
XR_246227.1:n.1485-207G= (AP4B1)
XM_011540523.3:c.1285+13G= (AP4B1) XP_011538825.1:n.1285+13G=
XM_011540525.3:c.1231+13G= (AP4B1) XP_011538827.1:n.1231+13G=
XM_017000089.2:c.1199-207G= (AP4B1) XP_016855578.1:n.1199-207G=
XM_017000090.1:c.1006+13G= (AP4B1) XP_016855579.1:n.1006+13G=
XM_017000091.2:c.920-207G= (AP4B1) XP_016855580.1:n.920-207G=
XM_017000092.2:c.535+13G= (AP4B1) XP_016855581.1:n.535+13G=
XM_024452422.1:c.1231+13G= (AP4B1) XP_024308190.1:n.1231+13G=
XM_024452423.1:c.1199-207G= (AP4B1) XP_024308191.1:n.1199-207G=
XM_024452435.1:c.974-207G= (AP4B1) XP_024308203.1:n.974-207G=
XM_024452441.1:c.695-207G= (AP4B1) XP_024308209.1:n.695-207G=
XR_001736928.2:n.1940+13G= (AP4B1)
XR_001736930.2:n.2084+13G= (AP4B1)
XR_002958805.1:n.1505-207G= (AP4B1)
XR_002958806.1:n.1981+13G= (AP4B1)
XR_002958807.1:n.1833G= (AP4B1)
NM_001253852.3:c.1510+13G= (AP4B1) MANE Select NP_001240781.1:n.1510+13G=
NM_001253853.3:c.1213+13G= (AP4B1) NP_001240782.1:n.1213+13G=
NM_001308312.2:c.1006+13G= (AP4B1) NP_001295241.1:n.1006+13G=
NM_006594.5:c.1510+13G= (AP4B1) NP_006585.2:n.1510+13G=