Canonical Allele Identifier: CA341714035

Gene: AP4B1 AP4B1-AS1

Linked Data

• MyVariant Identifiers: chr1:g.114442997G>C (hg19) ; chr1:g.113900375G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113900375G>C , CM000663.2:g.113900375G>C	GRCh38
NC_000001.10:g.114442997G>C , CM000663.1:g.114442997G>C	GRCh37
NC_000001.9:g.114244520G>C	NCBI36
NG_031901.1:g.9745C>G
NG_057565.1:g.757G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.418C>G (AP4B1)	ENSP00000358577.2:p.Gln140Glu
ENST00000369567.6:c.139C>G (AP4B1)	ENSP00000358580.1:p.Gln47Glu
ENST00000369571.3:c.643C>G (AP4B1)	ENSP00000358584.3:p.Gln215Glu
ENST00000432415.6:c.139C>G (AP4B1)	ENSP00000393622.2:p.Gln47Glu
ENST00000460653.2:c.643C>G (AP4B1)	ENSP00000518881.1:p.Gln215Glu
ENST00000484201.6:c.418C>G (AP4B1)	ENSP00000518883.1:p.Gln140Glu
ENST00000489092.6:c.*311C>G (AP4B1)	ENSP00000518884.1:n.*311C>G
ENST00000489499.6:c.495C>G (AP4B1)	ENSP00000518882.1:p.Ala165=
ENST00000713588.1:c.643C>G (AP4B1)	ENSP00000518880.1:p.Gln215Glu
ENST00000713590.1:c.643C>G (AP4B1)	ENSP00000518886.1:p.Gln215Glu
ENST00000369569.6:c.643C>G (AP4B1) MANE Select	ENSP00000358582.1:p.Gln215Glu
ENST00000256658.8:c.643C>G (AP4B1)	ENSP00000256658.4:p.Gln215Glu
ENST00000369564.5:c.418C>G (AP4B1)	ENSP00000358577.1:p.Gln140Glu
ENST00000369567.5:c.139C>G (AP4B1)	ENSP00000358580.1:p.Gln47Glu
ENST00000369569.5:c.643C>G (AP4B1)	ENSP00000358582.1:p.Gln215Glu
ENST00000369571.2:c.643C>G (AP4B1)	ENSP00000358584.2:p.Gln215Glu
ENST00000432415.5:c.139C>G (AP4B1)	ENSP00000393622.1:p.Gln47Glu
ENST00000472122.1:n.539C>G (AP4B1)
ENST00000484201.5:n.609C>G (AP4B1)
ENST00000489092.5:n.642C>G (AP4B1)
ENST00000489499.5:n.611C>G (AP4B1)
NM_001253852.1:c.643C>G (AP4B1)	NP_001240781.1:p.Gln215Glu
NM_001253852.2:c.643C>G (AP4B1)	NP_001240781.1:p.Gln215Glu
NM_001253853.1:c.346C>G (AP4B1)	NP_001240782.1:p.Gln116Glu
NM_001253853.2:c.346C>G (AP4B1)	NP_001240782.1:p.Gln116Glu
NM_001308312.1:c.139C>G (AP4B1)	NP_001295241.1:p.Gln47Glu
NM_006594.3:c.643C>G (AP4B1)	NP_006585.2:p.Gln215Glu
NM_006594.4:c.643C>G (AP4B1)	NP_006585.2:p.Gln215Glu
NR_037864.1:n.872G>C (AP4B1-AS1)
NR_125965.1:n.1040G>C (AP4B1-AS1)
XM_005270381.2:c.643C>G (AP4B1)	XP_005270438.1:p.Gln215Glu
XM_005270382.3:c.643C>G (AP4B1)	XP_005270439.1:p.Gln215Glu
XM_011540523.1:c.418C>G (AP4B1)	XP_011538825.1:p.Gln140Glu
XM_011540524.1:c.418C>G (AP4B1)	XP_011538826.1:p.Gln140Glu
XM_011540525.1:c.364C>G (AP4B1)	XP_011538827.1:p.Gln122Glu
XM_011540527.1:c.25C>G (AP4B1)	XP_011538829.1:p.Gln9Glu
XR_246227.1:n.825C>G (AP4B1)
XR_246228.2:n.825C>G (AP4B1)
XM_011540523.3:c.418C>G (AP4B1)	XP_011538825.1:p.Gln140Glu
XM_011540525.3:c.364C>G (AP4B1)	XP_011538827.1:p.Gln122Glu
XM_017000089.2:c.643C>G (AP4B1)	XP_016855578.1:p.Gln215Glu
XM_017000090.1:c.139C>G (AP4B1)	XP_016855579.1:p.Gln47Glu
XM_017000091.2:c.364C>G (AP4B1)	XP_016855580.1:p.Gln122Glu
XM_017000092.2:c.-602C>G (AP4B1)	XP_016855581.1:n.-602C>G
XM_017000093.2:c.643C>G (AP4B1)	XP_016855582.1:p.Gln215Glu
XM_024452422.1:c.364C>G (AP4B1)	XP_024308190.1:p.Gln122Glu
XM_024452423.1:c.643C>G (AP4B1)	XP_024308191.1:p.Gln215Glu
XM_024452435.1:c.418C>G (AP4B1)	XP_024308203.1:p.Gln140Glu
XM_024452441.1:c.139C>G (AP4B1)	XP_024308209.1:p.Gln47Glu
XR_001736928.2:n.845C>G (AP4B1)
XR_001736930.2:n.845C>G (AP4B1)
XR_002958805.1:n.845C>G (AP4B1)
XR_002958806.1:n.845C>G (AP4B1)
XR_002958807.1:n.725C>G (AP4B1)
NM_001253852.3:c.643C>G (AP4B1) MANE Select	NP_001240781.1:p.Gln215Glu
NM_001253853.3:c.346C>G (AP4B1)	NP_001240782.1:p.Gln116Glu
NM_001308312.2:c.139C>G (AP4B1)	NP_001295241.1:p.Gln47Glu
NM_006594.5:c.643C>G (AP4B1)	NP_006585.2:p.Gln215Glu