Canonical Allele Identifier: CA1189946100

Gene: AP4B1 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113896437C= , CM000663.2:g.113896437C=	GRCh38
NC_000001.10:g.114439059C= , CM000663.1:g.114439059C=	GRCh37
NC_000001.9:g.114240582C=	NCBI36
NG_031901.1:g.13683G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.1106G= (AP4B1)	ENSP00000358577.2:p.Gly369=
ENST00000369567.6:c.827G= (AP4B1)	ENSP00000358580.1:p.Gly276=
ENST00000369571.3:c.1331G= (AP4B1)	ENSP00000358584.3:p.Gly444=
ENST00000432415.6:c.827G= (AP4B1)	ENSP00000393622.2:p.Gly276=
ENST00000460653.2:c.*401G= (AP4B1)	ENSP00000518881.1:n.*401G=
ENST00000484201.6:c.*81G= (AP4B1)	ENSP00000518883.1:n.*81G=
ENST00000489499.6:c.*673G= (AP4B1)	ENSP00000518882.1:n.*673G=
ENST00000713588.1:c.*442G= (AP4B1)	ENSP00000518880.1:n.*442G=
ENST00000713590.1:c.1331G= (AP4B1)	ENSP00000518886.1:p.Gly444=
ENST00000369569.6:c.1331G= (AP4B1) MANE Select	ENSP00000358582.1:p.Gly444=
ENST00000256658.8:c.1331G= (AP4B1)	ENSP00000256658.4:p.Gly444=
ENST00000369567.5:c.827G= (AP4B1)	ENSP00000358580.1:p.Gly276=
ENST00000369569.5:c.1331G= (AP4B1)	ENSP00000358582.1:p.Gly444=
ENST00000462591.1:n.1503G= (AP4B1)
ENST00000479285.5:n.559G= (AP4B1)
ENST00000479801.1:n.165G= (AP4B1)
ENST00000484201.5:n.893G= (AP4B1)
NM_001253852.1:c.1331G= (AP4B1)	NP_001240781.1:p.Gly444=
NM_001253852.2:c.1331G= (AP4B1)	NP_001240781.1:p.Gly444=
NM_001253853.1:c.1034G= (AP4B1)	NP_001240782.1:p.Gly345=
NM_001253853.2:c.1034G= (AP4B1)	NP_001240782.1:p.Gly345=
NM_001308312.1:c.827G= (AP4B1)	NP_001295241.1:p.Gly276=
NM_006594.3:c.1331G= (AP4B1)	NP_006585.2:p.Gly444=
NM_006594.4:c.1331G= (AP4B1)	NP_006585.2:p.Gly444=
NR_037864.1:n.247-1431C= (AP4B1-AS1)
NR_125965.1:n.415-1431C= (AP4B1-AS1)
XM_005270381.2:c.1199-399G= (AP4B1)	XP_005270438.1:n.1199-399G=
XM_011540523.1:c.1106G= (AP4B1)	XP_011538825.1:p.Gly369=
XM_011540524.1:c.1106G= (AP4B1)	XP_011538826.1:p.Gly369=
XM_011540525.1:c.1052G= (AP4B1)	XP_011538827.1:p.Gly351=
XM_011540527.1:c.713G= (AP4B1)	XP_011538829.1:p.Gly238=
XM_011540528.1:c.356G= (AP4B1)	XP_011538830.1:p.Gly119=
XR_246227.1:n.1485-399G= (AP4B1)
XM_011540523.3:c.1106G= (AP4B1)	XP_011538825.1:p.Gly369=
XM_011540525.3:c.1052G= (AP4B1)	XP_011538827.1:p.Gly351=
XM_017000089.2:c.1199-399G= (AP4B1)	XP_016855578.1:n.1199-399G=
XM_017000090.1:c.827G= (AP4B1)	XP_016855579.1:p.Gly276=
XM_017000091.2:c.920-399G= (AP4B1)	XP_016855580.1:n.920-399G=
XM_017000092.2:c.356G= (AP4B1)	XP_016855581.1:p.Gly119=
XM_024452422.1:c.1052G= (AP4B1)	XP_024308190.1:p.Gly351=
XM_024452423.1:c.1199-399G= (AP4B1)	XP_024308191.1:n.1199-399G=
XM_024452435.1:c.974-399G= (AP4B1)	XP_024308203.1:n.974-399G=
XM_024452441.1:c.695-399G= (AP4B1)	XP_024308209.1:n.695-399G=
XR_001736928.2:n.1761G= (AP4B1)
XR_001736930.2:n.1905G= (AP4B1)
XR_002958805.1:n.1505-399G= (AP4B1)
XR_002958806.1:n.1802G= (AP4B1)
XR_002958807.1:n.1641G= (AP4B1)
NM_001253852.3:c.1331G= (AP4B1) MANE Select	NP_001240781.1:p.Gly444=
NM_001253853.3:c.1034G= (AP4B1)	NP_001240782.1:p.Gly345=
NM_001308312.2:c.827G= (AP4B1)	NP_001295241.1:p.Gly276=
NM_006594.5:c.1331G= (AP4B1)	NP_006585.2:p.Gly444=