Canonical Allele Identifier: CA341713905

Gene: AP4B1 AP4B1-AS1

Linked Data

• MyVariant Identifiers: chr1:g.114442960G>C (hg19) ; chr1:g.113900338G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113900338G>C , CM000663.2:g.113900338G>C	GRCh38
NC_000001.10:g.114442960G>C , CM000663.1:g.114442960G>C	GRCh37
NC_000001.9:g.114244483G>C	NCBI36
NG_031901.1:g.9782C>G
NG_057565.1:g.720G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.455C>G (AP4B1)	ENSP00000358577.2:p.Pro152Arg
ENST00000369567.6:c.176C>G (AP4B1)	ENSP00000358580.1:p.Pro59Arg
ENST00000369571.3:c.680C>G (AP4B1)	ENSP00000358584.3:p.Pro227Arg
ENST00000432415.6:c.176C>G (AP4B1)	ENSP00000393622.2:p.Pro59Arg
ENST00000460653.2:c.680C>G (AP4B1)	ENSP00000518881.1:p.Pro227Arg
ENST00000484201.6:c.455C>G (AP4B1)	ENSP00000518883.1:p.Pro152Arg
ENST00000489092.6:c.*348C>G (AP4B1)	ENSP00000518884.1:n.*348C>G
ENST00000489499.6:c.*22C>G (AP4B1)	ENSP00000518882.1:n.*22C>G
ENST00000713588.1:c.680C>G (AP4B1)	ENSP00000518880.1:p.Pro227Arg
ENST00000713590.1:c.680C>G (AP4B1)	ENSP00000518886.1:p.Pro227Arg
ENST00000369569.6:c.680C>G (AP4B1) MANE Select	ENSP00000358582.1:p.Pro227Arg
ENST00000256658.8:c.680C>G (AP4B1)	ENSP00000256658.4:p.Pro227Arg
ENST00000369564.5:c.455C>G (AP4B1)	ENSP00000358577.1:p.Pro152Arg
ENST00000369567.5:c.176C>G (AP4B1)	ENSP00000358580.1:p.Pro59Arg
ENST00000369569.5:c.680C>G (AP4B1)	ENSP00000358582.1:p.Pro227Arg
ENST00000369571.2:c.680C>G (AP4B1)	ENSP00000358584.2:p.Pro227Arg
ENST00000432415.5:c.176C>G (AP4B1)	ENSP00000393622.1:p.Pro59Arg
ENST00000472122.1:n.576C>G (AP4B1)
ENST00000484201.5:n.646C>G (AP4B1)
ENST00000489092.5:n.679C>G (AP4B1)
ENST00000489499.5:n.648C>G (AP4B1)
NM_001253852.1:c.680C>G (AP4B1)	NP_001240781.1:p.Pro227Arg
NM_001253852.2:c.680C>G (AP4B1)	NP_001240781.1:p.Pro227Arg
NM_001253853.1:c.383C>G (AP4B1)	NP_001240782.1:p.Pro128Arg
NM_001253853.2:c.383C>G (AP4B1)	NP_001240782.1:p.Pro128Arg
NM_001308312.1:c.176C>G (AP4B1)	NP_001295241.1:p.Pro59Arg
NM_006594.3:c.680C>G (AP4B1)	NP_006585.2:p.Pro227Arg
NM_006594.4:c.680C>G (AP4B1)	NP_006585.2:p.Pro227Arg
NR_037864.1:n.835G>C (AP4B1-AS1)
NR_125965.1:n.1003G>C (AP4B1-AS1)
XM_005270381.2:c.680C>G (AP4B1)	XP_005270438.1:p.Pro227Arg
XM_005270382.3:c.680C>G (AP4B1)	XP_005270439.1:p.Pro227Arg
XM_011540523.1:c.455C>G (AP4B1)	XP_011538825.1:p.Pro152Arg
XM_011540524.1:c.455C>G (AP4B1)	XP_011538826.1:p.Pro152Arg
XM_011540525.1:c.401C>G (AP4B1)	XP_011538827.1:p.Pro134Arg
XM_011540527.1:c.62C>G (AP4B1)	XP_011538829.1:p.Pro21Arg
XR_246227.1:n.862C>G (AP4B1)
XR_246228.2:n.862C>G (AP4B1)
XM_011540523.3:c.455C>G (AP4B1)	XP_011538825.1:p.Pro152Arg
XM_011540525.3:c.401C>G (AP4B1)	XP_011538827.1:p.Pro134Arg
XM_017000089.2:c.680C>G (AP4B1)	XP_016855578.1:p.Pro227Arg
XM_017000090.1:c.176C>G (AP4B1)	XP_016855579.1:p.Pro59Arg
XM_017000091.2:c.401C>G (AP4B1)	XP_016855580.1:p.Pro134Arg
XM_017000092.2:c.-565C>G (AP4B1)	XP_016855581.1:n.-565C>G
XM_017000093.2:c.680C>G (AP4B1)	XP_016855582.1:p.Pro227Arg
XM_024452422.1:c.401C>G (AP4B1)	XP_024308190.1:p.Pro134Arg
XM_024452423.1:c.680C>G (AP4B1)	XP_024308191.1:p.Pro227Arg
XM_024452435.1:c.455C>G (AP4B1)	XP_024308203.1:p.Pro152Arg
XM_024452441.1:c.176C>G (AP4B1)	XP_024308209.1:p.Pro59Arg
XR_001736928.2:n.882C>G (AP4B1)
XR_001736930.2:n.882C>G (AP4B1)
XR_002958805.1:n.882C>G (AP4B1)
XR_002958806.1:n.882C>G (AP4B1)
XR_002958807.1:n.762C>G (AP4B1)
NM_001253852.3:c.680C>G (AP4B1) MANE Select	NP_001240781.1:p.Pro227Arg
NM_001253853.3:c.383C>G (AP4B1)	NP_001240782.1:p.Pro128Arg
NM_001308312.2:c.176C>G (AP4B1)	NP_001295241.1:p.Pro59Arg
NM_006594.5:c.680C>G (AP4B1)	NP_006585.2:p.Pro227Arg