Canonical Allele Identifier: CA341710533

Gene: AP4B1 AP4B1-AS1

Linked Data

• MyVariant Identifiers: chr1:g.114439048C>G (hg19) ; chr1:g.113896426C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113896426C>G , CM000663.2:g.113896426C>G	GRCh38
NC_000001.10:g.114439048C>G , CM000663.1:g.114439048C>G	GRCh37
NC_000001.9:g.114240571C>G	NCBI36
NG_031901.1:g.13694G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.1117G>C (AP4B1)	ENSP00000358577.2:p.Glu373Gln
ENST00000369567.6:c.838G>C (AP4B1)	ENSP00000358580.1:p.Glu280Gln
ENST00000369571.3:c.1342G>C (AP4B1)	ENSP00000358584.3:p.Glu448Gln
ENST00000432415.6:c.838G>C (AP4B1)	ENSP00000393622.2:p.Glu280Gln
ENST00000460653.2:c.*412G>C (AP4B1)	ENSP00000518881.1:n.*412G>C
ENST00000484201.6:c.*92G>C (AP4B1)	ENSP00000518883.1:n.*92G>C
ENST00000489499.6:c.*684G>C (AP4B1)	ENSP00000518882.1:n.*684G>C
ENST00000713588.1:c.*453G>C (AP4B1)	ENSP00000518880.1:n.*453G>C
ENST00000713590.1:c.1342G>C (AP4B1)	ENSP00000518886.1:p.Glu448Gln
ENST00000369569.6:c.1342G>C (AP4B1) MANE Select	ENSP00000358582.1:p.Glu448Gln
ENST00000256658.8:c.1342G>C (AP4B1)	ENSP00000256658.4:p.Glu448Gln
ENST00000369567.5:c.838G>C (AP4B1)	ENSP00000358580.1:p.Glu280Gln
ENST00000369569.5:c.1342G>C (AP4B1)	ENSP00000358582.1:p.Glu448Gln
ENST00000462591.1:n.1514G>C (AP4B1)
ENST00000479285.5:n.570G>C (AP4B1)
ENST00000479801.1:n.176G>C (AP4B1)
ENST00000484201.5:n.904G>C (AP4B1)
NM_001253852.1:c.1342G>C (AP4B1)	NP_001240781.1:p.Glu448Gln
NM_001253852.2:c.1342G>C (AP4B1)	NP_001240781.1:p.Glu448Gln
NM_001253853.1:c.1045G>C (AP4B1)	NP_001240782.1:p.Glu349Gln
NM_001253853.2:c.1045G>C (AP4B1)	NP_001240782.1:p.Glu349Gln
NM_001308312.1:c.838G>C (AP4B1)	NP_001295241.1:p.Glu280Gln
NM_006594.3:c.1342G>C (AP4B1)	NP_006585.2:p.Glu448Gln
NM_006594.4:c.1342G>C (AP4B1)	NP_006585.2:p.Glu448Gln
NR_037864.1:n.247-1442C>G (AP4B1-AS1)
NR_125965.1:n.415-1442C>G (AP4B1-AS1)
XM_005270381.2:c.1199-388G>C (AP4B1)	XP_005270438.1:n.1199-388G>C
XM_011540523.1:c.1117G>C (AP4B1)	XP_011538825.1:p.Glu373Gln
XM_011540524.1:c.1117G>C (AP4B1)	XP_011538826.1:p.Glu373Gln
XM_011540525.1:c.1063G>C (AP4B1)	XP_011538827.1:p.Glu355Gln
XM_011540527.1:c.724G>C (AP4B1)	XP_011538829.1:p.Glu242Gln
XM_011540528.1:c.367G>C (AP4B1)	XP_011538830.1:p.Glu123Gln
XR_246227.1:n.1485-388G>C (AP4B1)
XM_011540523.3:c.1117G>C (AP4B1)	XP_011538825.1:p.Glu373Gln
XM_011540525.3:c.1063G>C (AP4B1)	XP_011538827.1:p.Glu355Gln
XM_017000089.2:c.1199-388G>C (AP4B1)	XP_016855578.1:n.1199-388G>C
XM_017000090.1:c.838G>C (AP4B1)	XP_016855579.1:p.Glu280Gln
XM_017000091.2:c.920-388G>C (AP4B1)	XP_016855580.1:n.920-388G>C
XM_017000092.2:c.367G>C (AP4B1)	XP_016855581.1:p.Glu123Gln
XM_024452422.1:c.1063G>C (AP4B1)	XP_024308190.1:p.Glu355Gln
XM_024452423.1:c.1199-388G>C (AP4B1)	XP_024308191.1:n.1199-388G>C
XM_024452435.1:c.974-388G>C (AP4B1)	XP_024308203.1:n.974-388G>C
XM_024452441.1:c.695-388G>C (AP4B1)	XP_024308209.1:n.695-388G>C
XR_001736928.2:n.1772G>C (AP4B1)
XR_001736930.2:n.1916G>C (AP4B1)
XR_002958805.1:n.1505-388G>C (AP4B1)
XR_002958806.1:n.1813G>C (AP4B1)
XR_002958807.1:n.1652G>C (AP4B1)
NM_001253852.3:c.1342G>C (AP4B1) MANE Select	NP_001240781.1:p.Glu448Gln
NM_001253853.3:c.1045G>C (AP4B1)	NP_001240782.1:p.Glu349Gln
NM_001308312.2:c.838G>C (AP4B1)	NP_001295241.1:p.Glu280Gln
NM_006594.5:c.1342G>C (AP4B1)	NP_006585.2:p.Glu448Gln