Canonical Allele Identifier: CA341711671

Gene: AP4B1 AP4B1-AS1

Linked Data

• MyVariant Identifiers: chr1:g.114441387T>A (hg19) ; chr1:g.113898765T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113898765T>A , CM000663.2:g.113898765T>A	GRCh38
NC_000001.10:g.114441387T>A , CM000663.1:g.114441387T>A	GRCh37
NC_000001.9:g.114242910T>A	NCBI36
NG_031901.1:g.11355A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.926A>T (AP4B1)	ENSP00000358577.2:p.Gln309Leu
ENST00000369567.6:c.647A>T (AP4B1)	ENSP00000358580.1:p.Gln216Leu
ENST00000369571.3:c.1151A>T (AP4B1)	ENSP00000358584.3:p.Gln384Leu
ENST00000432415.6:c.647A>T (AP4B1)	ENSP00000393622.2:p.Gln216Leu
ENST00000460653.2:c.*221A>T (AP4B1)	ENSP00000518881.1:n.*221A>T
ENST00000484201.6:c.524-2A>T (AP4B1)	ENSP00000518883.1:n.524-2A>T
ENST00000489499.6:c.*493A>T (AP4B1)	ENSP00000518882.1:n.*493A>T
ENST00000713588.1:c.*262A>T (AP4B1)	ENSP00000518880.1:n.*262A>T
ENST00000713590.1:c.1151A>T (AP4B1)	ENSP00000518886.1:p.Gln384Leu
ENST00000369569.6:c.1151A>T (AP4B1) MANE Select	ENSP00000358582.1:p.Gln384Leu
ENST00000256658.8:c.1151A>T (AP4B1)	ENSP00000256658.4:p.Gln384Leu
ENST00000369567.5:c.647A>T (AP4B1)	ENSP00000358580.1:p.Gln216Leu
ENST00000369569.5:c.1151A>T (AP4B1)	ENSP00000358582.1:p.Gln384Leu
ENST00000479285.5:n.379A>T (AP4B1)
ENST00000484201.5:n.715-2A>T (AP4B1)
NM_001253852.1:c.1151A>T (AP4B1)	NP_001240781.1:p.Gln384Leu
NM_001253852.2:c.1151A>T (AP4B1)	NP_001240781.1:p.Gln384Leu
NM_001253853.1:c.854A>T (AP4B1)	NP_001240782.1:p.Gln285Leu
NM_001253853.2:c.854A>T (AP4B1)	NP_001240782.1:p.Gln285Leu
NM_001308312.1:c.647A>T (AP4B1)	NP_001295241.1:p.Gln216Leu
NM_006594.3:c.1151A>T (AP4B1)	NP_006585.2:p.Gln384Leu
NM_006594.4:c.1151A>T (AP4B1)	NP_006585.2:p.Gln384Leu
NR_037864.1:n.368+776T>A (AP4B1-AS1)
NR_125965.1:n.536+776T>A (AP4B1-AS1)
XM_005270381.2:c.1151A>T (AP4B1)	XP_005270438.1:p.Gln384Leu
XM_005270382.3:c.1151A>T (AP4B1)	XP_005270439.1:p.Gln384Leu
XM_011540523.1:c.926A>T (AP4B1)	XP_011538825.1:p.Gln309Leu
XM_011540524.1:c.926A>T (AP4B1)	XP_011538826.1:p.Gln309Leu
XM_011540525.1:c.872A>T (AP4B1)	XP_011538827.1:p.Gln291Leu
XM_011540527.1:c.533A>T (AP4B1)	XP_011538829.1:p.Gln178Leu
XM_011540528.1:c.176A>T (AP4B1)	XP_011538830.1:p.Gln59Leu
XR_246227.1:n.1333A>T (AP4B1)
XR_246228.2:n.1561A>T (AP4B1)
XM_011540523.3:c.926A>T (AP4B1)	XP_011538825.1:p.Gln309Leu
XM_011540525.3:c.872A>T (AP4B1)	XP_011538827.1:p.Gln291Leu
XM_017000089.2:c.1151A>T (AP4B1)	XP_016855578.1:p.Gln384Leu
XM_017000090.1:c.647A>T (AP4B1)	XP_016855579.1:p.Gln216Leu
XM_017000091.2:c.872A>T (AP4B1)	XP_016855580.1:p.Gln291Leu
XM_017000092.2:c.176A>T (AP4B1)	XP_016855581.1:p.Gln59Leu
XM_017000093.2:c.1151A>T (AP4B1)	XP_016855582.1:p.Gln384Leu
XM_024452422.1:c.872A>T (AP4B1)	XP_024308190.1:p.Gln291Leu
XM_024452423.1:c.1151A>T (AP4B1)	XP_024308191.1:p.Gln384Leu
XM_024452435.1:c.926A>T (AP4B1)	XP_024308203.1:p.Gln309Leu
XM_024452441.1:c.647A>T (AP4B1)	XP_024308209.1:p.Gln216Leu
XR_001736928.2:n.1581A>T (AP4B1)
XR_001736930.2:n.1622A>T (AP4B1)
XR_002958805.1:n.1353A>T (AP4B1)
XR_002958806.1:n.1622A>T (AP4B1)
XR_002958807.1:n.1461A>T (AP4B1)
NM_001253852.3:c.1151A>T (AP4B1) MANE Select	NP_001240781.1:p.Gln384Leu
NM_001253853.3:c.854A>T (AP4B1)	NP_001240782.1:p.Gln285Leu
NM_001308312.2:c.647A>T (AP4B1)	NP_001295241.1:p.Gln216Leu
NM_006594.5:c.1151A>T (AP4B1)	NP_006585.2:p.Gln384Leu