Canonical Allele Identifier: CA1189946136

Gene: AP4B1 AP4B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113896514_113896516delinsAAC , CM000663.2:g.113896514_113896516delinsAAC	GRCh38
NC_000001.10:g.114439136_114439138delinsAAC , CM000663.1:g.114439136_114439138delinsAAC	GRCh37
NC_000001.9:g.114240659_114240661delinsAAC	NCBI36
NG_031901.1:g.13604_13606delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.1078-51_1078-49delinsGTT (AP4B1)	ENSP00000358577.2:n.1078-51_1078-49delinsGTT
ENST00000369567.6:c.799-51_799-49delinsGTT (AP4B1)	ENSP00000358580.1:n.799-51_799-49delinsGTT
ENST00000369571.3:c.1303-51_1303-49delinsGTT (AP4B1)	ENSP00000358584.3:n.1303-51_1303-49delinsGTT
ENST00000432415.6:c.799-51_799-49delinsGTT (AP4B1)	ENSP00000393622.2:n.799-51_799-49delinsGTT
ENST00000460653.2:c.*373-51_*373-49delinsGTT (AP4B1)	ENSP00000518881.1:n.*373-51_*373-49delinsGTT
ENST00000484201.6:c.*53-51_*53-49delinsGTT (AP4B1)	ENSP00000518883.1:n.*53-51_*53-49delinsGTT
ENST00000489499.6:c.*645-51_*645-49delinsGTT (AP4B1)	ENSP00000518882.1:n.*645-51_*645-49delinsGTT
ENST00000713588.1:c.*414-51_*414-49delinsGTT (AP4B1)	ENSP00000518880.1:n.*414-51_*414-49delinsGTT
ENST00000713590.1:c.1303-51_1303-49delinsGTT (AP4B1)	ENSP00000518886.1:n.1303-51_1303-49delinsGTT
ENST00000369569.6:c.1303-51_1303-49delinsGTT (AP4B1) MANE Select	ENSP00000358582.1:n.1303-51_1303-49delinsGTT
ENST00000256658.8:c.1303-51_1303-49delinsGTT (AP4B1)	ENSP00000256658.4:n.1303-51_1303-49delinsGTT
ENST00000369567.5:c.799-51_799-49delinsGTT (AP4B1)	ENSP00000358580.1:n.799-51_799-49delinsGTT
ENST00000369569.5:c.1303-51_1303-49delinsGTT (AP4B1)	ENSP00000358582.1:n.1303-51_1303-49delinsGTT
ENST00000462591.1:n.1424_1426delinsGTT (AP4B1)
ENST00000479285.5:n.531-51_531-49delinsGTT (AP4B1)
ENST00000479801.1:n.137-51_137-49delinsGTT (AP4B1)
ENST00000484201.5:n.865-51_865-49delinsGTT (AP4B1)
NM_001253852.1:c.1303-51_1303-49delinsGTT (AP4B1)	NP_001240781.1:n.1303-51_1303-49delinsGTT
NM_001253852.2:c.1303-51_1303-49delinsGTT (AP4B1)	NP_001240781.1:n.1303-51_1303-49delinsGTT
NM_001253853.1:c.1006-51_1006-49delinsGTT (AP4B1)	NP_001240782.1:n.1006-51_1006-49delinsGTT
NM_001253853.2:c.1006-51_1006-49delinsGTT (AP4B1)	NP_001240782.1:n.1006-51_1006-49delinsGTT
NM_001308312.1:c.799-51_799-49delinsGTT (AP4B1)	NP_001295241.1:n.799-51_799-49delinsGTT
NM_006594.3:c.1303-51_1303-49delinsGTT (AP4B1)	NP_006585.2:n.1303-51_1303-49delinsGTT
NM_006594.4:c.1303-51_1303-49delinsGTT (AP4B1)	NP_006585.2:n.1303-51_1303-49delinsGTT
NR_037864.1:n.247-1354_247-1352delinsAAC (AP4B1-AS1)
NR_125965.1:n.415-1354_415-1352delinsAAC (AP4B1-AS1)
XM_005270381.2:c.1199-478_1199-476delinsGTT (AP4B1)	XP_005270438.1:n.1199-478_1199-476delinsGTT
XM_011540523.1:c.1078-51_1078-49delinsGTT (AP4B1)	XP_011538825.1:n.1078-51_1078-49delinsGTT
XM_011540524.1:c.1078-51_1078-49delinsGTT (AP4B1)	XP_011538826.1:n.1078-51_1078-49delinsGTT
XM_011540525.1:c.1024-51_1024-49delinsGTT (AP4B1)	XP_011538827.1:n.1024-51_1024-49delinsGTT
XM_011540527.1:c.685-51_685-49delinsGTT (AP4B1)	XP_011538829.1:n.685-51_685-49delinsGTT
XM_011540528.1:c.328-51_328-49delinsGTT (AP4B1)	XP_011538830.1:n.328-51_328-49delinsGTT
XR_246227.1:n.1485-478_1485-476delinsGTT (AP4B1)
XM_011540523.3:c.1078-51_1078-49delinsGTT (AP4B1)	XP_011538825.1:n.1078-51_1078-49delinsGTT
XM_011540525.3:c.1024-51_1024-49delinsGTT (AP4B1)	XP_011538827.1:n.1024-51_1024-49delinsGTT
XM_017000089.2:c.1199-478_1199-476delinsGTT (AP4B1)	XP_016855578.1:n.1199-478_1199-476delinsGTT
XM_017000090.1:c.799-51_799-49delinsGTT (AP4B1)	XP_016855579.1:n.799-51_799-49delinsGTT
XM_017000091.2:c.920-478_920-476delinsGTT (AP4B1)	XP_016855580.1:n.920-478_920-476delinsGTT
XM_017000092.2:c.328-51_328-49delinsGTT (AP4B1)	XP_016855581.1:n.328-51_328-49delinsGTT
XM_024452422.1:c.1024-51_1024-49delinsGTT (AP4B1)	XP_024308190.1:n.1024-51_1024-49delinsGTT
XM_024452423.1:c.1199-478_1199-476delinsGTT (AP4B1)	XP_024308191.1:n.1199-478_1199-476delinsGTT
XM_024452435.1:c.974-478_974-476delinsGTT (AP4B1)	XP_024308203.1:n.974-478_974-476delinsGTT
XM_024452441.1:c.695-478_695-476delinsGTT (AP4B1)	XP_024308209.1:n.695-478_695-476delinsGTT
XR_001736928.2:n.1733-51_1733-49delinsGTT (AP4B1)
XR_001736930.2:n.1877-51_1877-49delinsGTT (AP4B1)
XR_002958805.1:n.1505-478_1505-476delinsGTT (AP4B1)
XR_002958806.1:n.1774-51_1774-49delinsGTT (AP4B1)
XR_002958807.1:n.1613-51_1613-49delinsGTT (AP4B1)
NM_001253852.3:c.1303-51_1303-49delinsGTT (AP4B1) MANE Select	NP_001240781.1:n.1303-51_1303-49delinsGTT
NM_001253853.3:c.1006-51_1006-49delinsGTT (AP4B1)	NP_001240782.1:n.1006-51_1006-49delinsGTT
NM_001308312.2:c.799-51_799-49delinsGTT (AP4B1)	NP_001295241.1:n.799-51_799-49delinsGTT
NM_006594.5:c.1303-51_1303-49delinsGTT (AP4B1)	NP_006585.2:n.1303-51_1303-49delinsGTT