Canonical Allele Identifier: CA341713463

Gene: AP4B1 AP4B1-AS1

Linked Data

• MyVariant Identifiers: chr1:g.114442841G>T (hg19) ; chr1:g.113900219G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113900219G>T , CM000663.2:g.113900219G>T	GRCh38
NC_000001.10:g.114442841G>T , CM000663.1:g.114442841G>T	GRCh37
NC_000001.9:g.114244364G>T	NCBI36
NG_031901.1:g.9901C>A
NG_057565.1:g.601G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.574C>A (AP4B1)	ENSP00000358577.2:p.Pro192Thr
ENST00000369567.6:c.295C>A (AP4B1)	ENSP00000358580.1:p.Pro99Thr
ENST00000369571.3:c.799C>A (AP4B1)	ENSP00000358584.3:p.Pro267Thr
ENST00000432415.6:c.295C>A (AP4B1)	ENSP00000393622.2:p.Pro99Thr
ENST00000460653.2:c.799C>A (AP4B1)	ENSP00000518881.1:p.Pro267Thr
ENST00000484201.6:c.523+51C>A (AP4B1)	ENSP00000518883.1:n.523+51C>A
ENST00000489092.6:c.*467C>A (AP4B1)	ENSP00000518884.1:n.*467C>A
ENST00000489499.6:c.*141C>A (AP4B1)	ENSP00000518882.1:n.*141C>A
ENST00000713588.1:c.799C>A (AP4B1)	ENSP00000518880.1:p.Pro267Thr
ENST00000713590.1:c.799C>A (AP4B1)	ENSP00000518886.1:p.Pro267Thr
ENST00000369569.6:c.799C>A (AP4B1) MANE Select	ENSP00000358582.1:p.Pro267Thr
ENST00000256658.8:c.799C>A (AP4B1)	ENSP00000256658.4:p.Pro267Thr
ENST00000369564.5:c.574C>A (AP4B1)	ENSP00000358577.1:p.Pro192Thr
ENST00000369567.5:c.295C>A (AP4B1)	ENSP00000358580.1:p.Pro99Thr
ENST00000369569.5:c.799C>A (AP4B1)	ENSP00000358582.1:p.Pro267Thr
ENST00000432415.5:c.295C>A (AP4B1)	ENSP00000393622.1:p.Pro99Thr
ENST00000479285.5:n.27C>A (AP4B1)
ENST00000484201.5:n.714+51C>A (AP4B1)
ENST00000489092.5:n.798C>A (AP4B1)
ENST00000489499.5:n.767C>A (AP4B1)
NM_001253852.1:c.799C>A (AP4B1)	NP_001240781.1:p.Pro267Thr
NM_001253852.2:c.799C>A (AP4B1)	NP_001240781.1:p.Pro267Thr
NM_001253853.1:c.502C>A (AP4B1)	NP_001240782.1:p.Pro168Thr
NM_001253853.2:c.502C>A (AP4B1)	NP_001240782.1:p.Pro168Thr
NM_001308312.1:c.295C>A (AP4B1)	NP_001295241.1:p.Pro99Thr
NM_006594.3:c.799C>A (AP4B1)	NP_006585.2:p.Pro267Thr
NM_006594.4:c.799C>A (AP4B1)	NP_006585.2:p.Pro267Thr
NR_037864.1:n.716G>T (AP4B1-AS1)
NR_125965.1:n.884G>T (AP4B1-AS1)
XM_005270381.2:c.799C>A (AP4B1)	XP_005270438.1:p.Pro267Thr
XM_005270382.3:c.799C>A (AP4B1)	XP_005270439.1:p.Pro267Thr
XM_011540523.1:c.574C>A (AP4B1)	XP_011538825.1:p.Pro192Thr
XM_011540524.1:c.574C>A (AP4B1)	XP_011538826.1:p.Pro192Thr
XM_011540525.1:c.520C>A (AP4B1)	XP_011538827.1:p.Pro174Thr
XM_011540527.1:c.181C>A (AP4B1)	XP_011538829.1:p.Pro61Thr
XR_246227.1:n.981C>A (AP4B1)
XR_246228.2:n.981C>A (AP4B1)
XM_011540523.3:c.574C>A (AP4B1)	XP_011538825.1:p.Pro192Thr
XM_011540525.3:c.520C>A (AP4B1)	XP_011538827.1:p.Pro174Thr
XM_017000089.2:c.799C>A (AP4B1)	XP_016855578.1:p.Pro267Thr
XM_017000090.1:c.295C>A (AP4B1)	XP_016855579.1:p.Pro99Thr
XM_017000091.2:c.520C>A (AP4B1)	XP_016855580.1:p.Pro174Thr
XM_017000092.2:c.-446C>A (AP4B1)	XP_016855581.1:n.-446C>A
XM_017000093.2:c.799C>A (AP4B1)	XP_016855582.1:p.Pro267Thr
XM_024452422.1:c.520C>A (AP4B1)	XP_024308190.1:p.Pro174Thr
XM_024452423.1:c.799C>A (AP4B1)	XP_024308191.1:p.Pro267Thr
XM_024452435.1:c.574C>A (AP4B1)	XP_024308203.1:p.Pro192Thr
XM_024452441.1:c.295C>A (AP4B1)	XP_024308209.1:p.Pro99Thr
XR_001736928.2:n.1001C>A (AP4B1)
XR_001736930.2:n.1001C>A (AP4B1)
XR_002958805.1:n.1001C>A (AP4B1)
XR_002958806.1:n.1001C>A (AP4B1)
XR_002958807.1:n.881C>A (AP4B1)
NM_001253852.3:c.799C>A (AP4B1) MANE Select	NP_001240781.1:p.Pro267Thr
NM_001253853.3:c.502C>A (AP4B1)	NP_001240782.1:p.Pro168Thr
NM_001308312.2:c.295C>A (AP4B1)	NP_001295241.1:p.Pro99Thr
NM_006594.5:c.799C>A (AP4B1)	NP_006585.2:p.Pro267Thr