Canonical Allele Identifier: CA2647213644

Gene: AP4B1 AP4B1-AS1

Linked Data

• gnomAD v4: 1-113896138-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113896138A>C , CM000663.2:g.113896138A>C	GRCh38
NC_000001.10:g.114438760A>C , CM000663.1:g.114438760A>C	GRCh37
NC_000001.9:g.114240283A>C	NCBI36
NG_031901.1:g.13982T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.1286-100T>G (AP4B1)	ENSP00000358577.2:n.1286-100T>G
ENST00000369567.6:c.1007-100T>G (AP4B1)	ENSP00000358580.1:n.1007-100T>G
ENST00000369571.3:c.1511-100T>G (AP4B1)	ENSP00000358584.3:n.1511-100T>G
ENST00000432415.6:c.1007-100T>G (AP4B1)	ENSP00000393622.2:n.1007-100T>G
ENST00000460653.2:c.*581-100T>G (AP4B1)	ENSP00000518881.1:n.*581-100T>G
ENST00000484201.6:c.*261-100T>G (AP4B1)	ENSP00000518883.1:n.*261-100T>G
ENST00000489499.6:c.*853-100T>G (AP4B1)	ENSP00000518882.1:n.*853-100T>G
ENST00000713588.1:c.*622-100T>G (AP4B1)	ENSP00000518880.1:n.*622-100T>G
ENST00000713590.1:c.1511-100T>G (AP4B1)	ENSP00000518886.1:n.1511-100T>G
ENST00000369569.6:c.1511-100T>G (AP4B1) MANE Select	ENSP00000358582.1:n.1511-100T>G
ENST00000256658.8:c.1511-100T>G (AP4B1)	ENSP00000256658.4:n.1511-100T>G
ENST00000369567.5:c.1007-100T>G (AP4B1)	ENSP00000358580.1:n.1007-100T>G
ENST00000369569.5:c.1511-100T>G (AP4B1)	ENSP00000358582.1:n.1511-100T>G
ENST00000462591.1:n.1683-100T>G (AP4B1)
ENST00000479285.5:n.858T>G (AP4B1)
ENST00000479801.1:n.464T>G (AP4B1)
NM_001253852.1:c.1511-100T>G (AP4B1)	NP_001240781.1:n.1511-100T>G
NM_001253852.2:c.1511-100T>G (AP4B1)	NP_001240781.1:n.1511-100T>G
NM_001253853.1:c.1214-100T>G (AP4B1)	NP_001240782.1:n.1214-100T>G
NM_001253853.2:c.1214-100T>G (AP4B1)	NP_001240782.1:n.1214-100T>G
NM_001308312.1:c.1007-100T>G (AP4B1)	NP_001295241.1:n.1007-100T>G
NM_006594.3:c.1511-100T>G (AP4B1)	NP_006585.2:n.1511-100T>G
NM_006594.4:c.1511-100T>G (AP4B1)	NP_006585.2:n.1511-100T>G
NR_037864.1:n.247-1730A>C (AP4B1-AS1)
NR_125965.1:n.415-1730A>C (AP4B1-AS1)
XM_005270381.2:c.1199-100T>G (AP4B1)	XP_005270438.1:n.1199-100T>G
XM_011540523.1:c.1286-100T>G (AP4B1)	XP_011538825.1:n.1286-100T>G
XM_011540524.1:c.1286-100T>G (AP4B1)	XP_011538826.1:n.1286-100T>G
XM_011540525.1:c.1232-100T>G (AP4B1)	XP_011538827.1:n.1232-100T>G
XM_011540527.1:c.893-100T>G (AP4B1)	XP_011538829.1:n.893-100T>G
XM_011540528.1:c.536-100T>G (AP4B1)	XP_011538830.1:n.536-100T>G
XR_246227.1:n.1485-100T>G (AP4B1)
XM_011540523.3:c.1286-100T>G (AP4B1)	XP_011538825.1:n.1286-100T>G
XM_011540525.3:c.1232-100T>G (AP4B1)	XP_011538827.1:n.1232-100T>G
XM_017000089.2:c.1199-100T>G (AP4B1)	XP_016855578.1:n.1199-100T>G
XM_017000090.1:c.1007-100T>G (AP4B1)	XP_016855579.1:n.1007-100T>G
XM_017000091.2:c.920-100T>G (AP4B1)	XP_016855580.1:n.920-100T>G
XM_017000092.2:c.536-100T>G (AP4B1)	XP_016855581.1:n.536-100T>G
XM_024452422.1:c.1232-100T>G (AP4B1)	XP_024308190.1:n.1232-100T>G
XM_024452423.1:c.1199-100T>G (AP4B1)	XP_024308191.1:n.1199-100T>G
XM_024452435.1:c.974-100T>G (AP4B1)	XP_024308203.1:n.974-100T>G
XM_024452441.1:c.695-100T>G (AP4B1)	XP_024308209.1:n.695-100T>G
XR_001736928.2:n.1941-100T>G (AP4B1)
XR_001736930.2:n.2085-100T>G (AP4B1)
XR_002958805.1:n.1505-100T>G (AP4B1)
XR_002958806.1:n.1982-100T>G (AP4B1)
XR_002958807.1:n.1940T>G (AP4B1)
NM_001253852.3:c.1511-100T>G (AP4B1) MANE Select	NP_001240781.1:n.1511-100T>G
NM_001253853.3:c.1214-100T>G (AP4B1)	NP_001240782.1:n.1214-100T>G
NM_001308312.2:c.1007-100T>G (AP4B1)	NP_001295241.1:n.1007-100T>G
NM_006594.5:c.1511-100T>G (AP4B1)	NP_006585.2:n.1511-100T>G