Canonical Allele Identifier: CA1189947599

Gene: AP4B1 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113900273G= , CM000663.2:g.113900273G=	GRCh38
NC_000001.10:g.114442895G= , CM000663.1:g.114442895G=	GRCh37
NC_000001.9:g.114244418G=	NCBI36
NG_031901.1:g.9847C=
NG_057565.1:g.655G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.520C= (AP4B1)	ENSP00000358577.2:p.Pro174=
ENST00000369567.6:c.241C= (AP4B1)	ENSP00000358580.1:p.Pro81=
ENST00000369571.3:c.745C= (AP4B1)	ENSP00000358584.3:p.Pro249=
ENST00000432415.6:c.241C= (AP4B1)	ENSP00000393622.2:p.Pro81=
ENST00000460653.2:c.745C= (AP4B1)	ENSP00000518881.1:p.Pro249=
ENST00000484201.6:c.520C= (AP4B1)	ENSP00000518883.1:p.Pro174=
ENST00000489092.6:c.*413C= (AP4B1)	ENSP00000518884.1:n.*413C=
ENST00000489499.6:c.*87C= (AP4B1)	ENSP00000518882.1:n.*87C=
ENST00000713588.1:c.745C= (AP4B1)	ENSP00000518880.1:p.Pro249=
ENST00000713590.1:c.745C= (AP4B1)	ENSP00000518886.1:p.Pro249=
ENST00000369569.6:c.745C= (AP4B1) MANE Select	ENSP00000358582.1:p.Pro249=
ENST00000256658.8:c.745C= (AP4B1)	ENSP00000256658.4:p.Pro249=
ENST00000369564.5:c.520C= (AP4B1)	ENSP00000358577.1:p.Pro174=
ENST00000369567.5:c.241C= (AP4B1)	ENSP00000358580.1:p.Pro81=
ENST00000369569.5:c.745C= (AP4B1)	ENSP00000358582.1:p.Pro249=
ENST00000369571.2:c.745C= (AP4B1)	ENSP00000358584.2:p.Pro249=
ENST00000432415.5:c.241C= (AP4B1)	ENSP00000393622.1:p.Pro81=
ENST00000484201.5:n.711C= (AP4B1)
ENST00000489092.5:n.744C= (AP4B1)
ENST00000489499.5:n.713C= (AP4B1)
NM_001253852.1:c.745C= (AP4B1)	NP_001240781.1:p.Pro249=
NM_001253852.2:c.745C= (AP4B1)	NP_001240781.1:p.Pro249=
NM_001253853.1:c.448C= (AP4B1)	NP_001240782.1:p.Pro150=
NM_001253853.2:c.448C= (AP4B1)	NP_001240782.1:p.Pro150=
NM_001308312.1:c.241C= (AP4B1)	NP_001295241.1:p.Pro81=
NM_006594.3:c.745C= (AP4B1)	NP_006585.2:p.Pro249=
NM_006594.4:c.745C= (AP4B1)	NP_006585.2:p.Pro249=
NR_037864.1:n.770G= (AP4B1-AS1)
NR_125965.1:n.938G= (AP4B1-AS1)
XM_005270381.2:c.745C= (AP4B1)	XP_005270438.1:p.Pro249=
XM_005270382.3:c.745C= (AP4B1)	XP_005270439.1:p.Pro249=
XM_011540523.1:c.520C= (AP4B1)	XP_011538825.1:p.Pro174=
XM_011540524.1:c.520C= (AP4B1)	XP_011538826.1:p.Pro174=
XM_011540525.1:c.466C= (AP4B1)	XP_011538827.1:p.Pro156=
XM_011540527.1:c.127C= (AP4B1)	XP_011538829.1:p.Pro43=
XR_246227.1:n.927C= (AP4B1)
XR_246228.2:n.927C= (AP4B1)
XM_011540523.3:c.520C= (AP4B1)	XP_011538825.1:p.Pro174=
XM_011540525.3:c.466C= (AP4B1)	XP_011538827.1:p.Pro156=
XM_017000089.2:c.745C= (AP4B1)	XP_016855578.1:p.Pro249=
XM_017000090.1:c.241C= (AP4B1)	XP_016855579.1:p.Pro81=
XM_017000091.2:c.466C= (AP4B1)	XP_016855580.1:p.Pro156=
XM_017000092.2:c.-500C= (AP4B1)	XP_016855581.1:n.-500C=
XM_017000093.2:c.745C= (AP4B1)	XP_016855582.1:p.Pro249=
XM_024452422.1:c.466C= (AP4B1)	XP_024308190.1:p.Pro156=
XM_024452423.1:c.745C= (AP4B1)	XP_024308191.1:p.Pro249=
XM_024452435.1:c.520C= (AP4B1)	XP_024308203.1:p.Pro174=
XM_024452441.1:c.241C= (AP4B1)	XP_024308209.1:p.Pro81=
XR_001736928.2:n.947C= (AP4B1)
XR_001736930.2:n.947C= (AP4B1)
XR_002958805.1:n.947C= (AP4B1)
XR_002958806.1:n.947C= (AP4B1)
XR_002958807.1:n.827C= (AP4B1)
NM_001253852.3:c.745C= (AP4B1) MANE Select	NP_001240781.1:p.Pro249=
NM_001253853.3:c.448C= (AP4B1)	NP_001240782.1:p.Pro150=
NM_001308312.2:c.241C= (AP4B1)	NP_001295241.1:p.Pro81=
NM_006594.5:c.745C= (AP4B1)	NP_006585.2:p.Pro249=