Canonical Allele Identifier: CA341710432

Gene: AP4B1 AP4B1-AS1

Linked Data

• MyVariant Identifiers: chr1:g.114439032G>T (hg19) ; chr1:g.113896410G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113896410G>T , CM000663.2:g.113896410G>T	GRCh38
NC_000001.10:g.114439032G>T , CM000663.1:g.114439032G>T	GRCh37
NC_000001.9:g.114240555G>T	NCBI36
NG_031901.1:g.13710C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.1133C>A (AP4B1)	ENSP00000358577.2:p.Ala378Asp
ENST00000369567.6:c.854C>A (AP4B1)	ENSP00000358580.1:p.Ala285Asp
ENST00000369571.3:c.1358C>A (AP4B1)	ENSP00000358584.3:p.Ala453Asp
ENST00000432415.6:c.854C>A (AP4B1)	ENSP00000393622.2:p.Ala285Asp
ENST00000460653.2:c.*428C>A (AP4B1)	ENSP00000518881.1:n.*428C>A
ENST00000484201.6:c.*108C>A (AP4B1)	ENSP00000518883.1:n.*108C>A
ENST00000489499.6:c.*700C>A (AP4B1)	ENSP00000518882.1:n.*700C>A
ENST00000713588.1:c.*469C>A (AP4B1)	ENSP00000518880.1:n.*469C>A
ENST00000713590.1:c.1358C>A (AP4B1)	ENSP00000518886.1:p.Ala453Asp
ENST00000369569.6:c.1358C>A (AP4B1) MANE Select	ENSP00000358582.1:p.Ala453Asp
ENST00000256658.8:c.1358C>A (AP4B1)	ENSP00000256658.4:p.Ala453Asp
ENST00000369567.5:c.854C>A (AP4B1)	ENSP00000358580.1:p.Ala285Asp
ENST00000369569.5:c.1358C>A (AP4B1)	ENSP00000358582.1:p.Ala453Asp
ENST00000462591.1:n.1530C>A (AP4B1)
ENST00000479285.5:n.586C>A (AP4B1)
ENST00000479801.1:n.192C>A (AP4B1)
ENST00000484201.5:n.920C>A (AP4B1)
NM_001253852.1:c.1358C>A (AP4B1)	NP_001240781.1:p.Ala453Asp
NM_001253852.2:c.1358C>A (AP4B1)	NP_001240781.1:p.Ala453Asp
NM_001253853.1:c.1061C>A (AP4B1)	NP_001240782.1:p.Ala354Asp
NM_001253853.2:c.1061C>A (AP4B1)	NP_001240782.1:p.Ala354Asp
NM_001308312.1:c.854C>A (AP4B1)	NP_001295241.1:p.Ala285Asp
NM_006594.3:c.1358C>A (AP4B1)	NP_006585.2:p.Ala453Asp
NM_006594.4:c.1358C>A (AP4B1)	NP_006585.2:p.Ala453Asp
NR_037864.1:n.247-1458G>T (AP4B1-AS1)
NR_125965.1:n.415-1458G>T (AP4B1-AS1)
XM_005270381.2:c.1199-372C>A (AP4B1)	XP_005270438.1:n.1199-372C>A
XM_011540523.1:c.1133C>A (AP4B1)	XP_011538825.1:p.Ala378Asp
XM_011540524.1:c.1133C>A (AP4B1)	XP_011538826.1:p.Ala378Asp
XM_011540525.1:c.1079C>A (AP4B1)	XP_011538827.1:p.Ala360Asp
XM_011540527.1:c.740C>A (AP4B1)	XP_011538829.1:p.Ala247Asp
XM_011540528.1:c.383C>A (AP4B1)	XP_011538830.1:p.Ala128Asp
XR_246227.1:n.1485-372C>A (AP4B1)
XM_011540523.3:c.1133C>A (AP4B1)	XP_011538825.1:p.Ala378Asp
XM_011540525.3:c.1079C>A (AP4B1)	XP_011538827.1:p.Ala360Asp
XM_017000089.2:c.1199-372C>A (AP4B1)	XP_016855578.1:n.1199-372C>A
XM_017000090.1:c.854C>A (AP4B1)	XP_016855579.1:p.Ala285Asp
XM_017000091.2:c.920-372C>A (AP4B1)	XP_016855580.1:n.920-372C>A
XM_017000092.2:c.383C>A (AP4B1)	XP_016855581.1:p.Ala128Asp
XM_024452422.1:c.1079C>A (AP4B1)	XP_024308190.1:p.Ala360Asp
XM_024452423.1:c.1199-372C>A (AP4B1)	XP_024308191.1:n.1199-372C>A
XM_024452435.1:c.974-372C>A (AP4B1)	XP_024308203.1:n.974-372C>A
XM_024452441.1:c.695-372C>A (AP4B1)	XP_024308209.1:n.695-372C>A
XR_001736928.2:n.1788C>A (AP4B1)
XR_001736930.2:n.1932C>A (AP4B1)
XR_002958805.1:n.1505-372C>A (AP4B1)
XR_002958806.1:n.1829C>A (AP4B1)
XR_002958807.1:n.1668C>A (AP4B1)
NM_001253852.3:c.1358C>A (AP4B1) MANE Select	NP_001240781.1:p.Ala453Asp
NM_001253853.3:c.1061C>A (AP4B1)	NP_001240782.1:p.Ala354Asp
NM_001308312.2:c.854C>A (AP4B1)	NP_001295241.1:p.Ala285Asp
NM_006594.5:c.1358C>A (AP4B1)	NP_006585.2:p.Ala453Asp