Canonical Allele Identifier: CA341710061

Gene: AP4B1 AP4B1-AS1

Linked Data

• MyVariant Identifiers: chr1:g.114438960A>G (hg19) ; chr1:g.113896338A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113896338A>G , CM000663.2:g.113896338A>G	GRCh38
NC_000001.10:g.114438960A>G , CM000663.1:g.114438960A>G	GRCh37
NC_000001.9:g.114240483A>G	NCBI36
NG_031901.1:g.13782T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.1205T>C (AP4B1)	ENSP00000358577.2:p.Leu402Pro
ENST00000369567.6:c.926T>C (AP4B1)	ENSP00000358580.1:p.Leu309Pro
ENST00000369571.3:c.1430T>C (AP4B1)	ENSP00000358584.3:p.Leu477Pro
ENST00000432415.6:c.926T>C (AP4B1)	ENSP00000393622.2:p.Leu309Pro
ENST00000460653.2:c.*500T>C (AP4B1)	ENSP00000518881.1:n.*500T>C
ENST00000484201.6:c.*180T>C (AP4B1)	ENSP00000518883.1:n.*180T>C
ENST00000489499.6:c.*772T>C (AP4B1)	ENSP00000518882.1:n.*772T>C
ENST00000713588.1:c.*541T>C (AP4B1)	ENSP00000518880.1:n.*541T>C
ENST00000713590.1:c.1430T>C (AP4B1)	ENSP00000518886.1:p.Leu477Pro
ENST00000369569.6:c.1430T>C (AP4B1) MANE Select	ENSP00000358582.1:p.Leu477Pro
ENST00000256658.8:c.1430T>C (AP4B1)	ENSP00000256658.4:p.Leu477Pro
ENST00000369567.5:c.926T>C (AP4B1)	ENSP00000358580.1:p.Leu309Pro
ENST00000369569.5:c.1430T>C (AP4B1)	ENSP00000358582.1:p.Leu477Pro
ENST00000462591.1:n.1602T>C (AP4B1)
ENST00000479285.5:n.658T>C (AP4B1)
ENST00000479801.1:n.264T>C (AP4B1)
NM_001253852.1:c.1430T>C (AP4B1)	NP_001240781.1:p.Leu477Pro
NM_001253852.2:c.1430T>C (AP4B1)	NP_001240781.1:p.Leu477Pro
NM_001253853.1:c.1133T>C (AP4B1)	NP_001240782.1:p.Leu378Pro
NM_001253853.2:c.1133T>C (AP4B1)	NP_001240782.1:p.Leu378Pro
NM_001308312.1:c.926T>C (AP4B1)	NP_001295241.1:p.Leu309Pro
NM_006594.3:c.1430T>C (AP4B1)	NP_006585.2:p.Leu477Pro
NM_006594.4:c.1430T>C (AP4B1)	NP_006585.2:p.Leu477Pro
NR_037864.1:n.247-1530A>G (AP4B1-AS1)
NR_125965.1:n.415-1530A>G (AP4B1-AS1)
XM_005270381.2:c.1199-300T>C (AP4B1)	XP_005270438.1:n.1199-300T>C
XM_011540523.1:c.1205T>C (AP4B1)	XP_011538825.1:p.Leu402Pro
XM_011540524.1:c.1205T>C (AP4B1)	XP_011538826.1:p.Leu402Pro
XM_011540525.1:c.1151T>C (AP4B1)	XP_011538827.1:p.Leu384Pro
XM_011540527.1:c.812T>C (AP4B1)	XP_011538829.1:p.Leu271Pro
XM_011540528.1:c.455T>C (AP4B1)	XP_011538830.1:p.Leu152Pro
XR_246227.1:n.1485-300T>C (AP4B1)
XM_011540523.3:c.1205T>C (AP4B1)	XP_011538825.1:p.Leu402Pro
XM_011540525.3:c.1151T>C (AP4B1)	XP_011538827.1:p.Leu384Pro
XM_017000089.2:c.1199-300T>C (AP4B1)	XP_016855578.1:n.1199-300T>C
XM_017000090.1:c.926T>C (AP4B1)	XP_016855579.1:p.Leu309Pro
XM_017000091.2:c.920-300T>C (AP4B1)	XP_016855580.1:n.920-300T>C
XM_017000092.2:c.455T>C (AP4B1)	XP_016855581.1:p.Leu152Pro
XM_024452422.1:c.1151T>C (AP4B1)	XP_024308190.1:p.Leu384Pro
XM_024452423.1:c.1199-300T>C (AP4B1)	XP_024308191.1:n.1199-300T>C
XM_024452435.1:c.974-300T>C (AP4B1)	XP_024308203.1:n.974-300T>C
XM_024452441.1:c.695-300T>C (AP4B1)	XP_024308209.1:n.695-300T>C
XR_001736928.2:n.1860T>C (AP4B1)
XR_001736930.2:n.2004T>C (AP4B1)
XR_002958805.1:n.1505-300T>C (AP4B1)
XR_002958806.1:n.1901T>C (AP4B1)
XR_002958807.1:n.1740T>C (AP4B1)
NM_001253852.3:c.1430T>C (AP4B1) MANE Select	NP_001240781.1:p.Leu477Pro
NM_001253853.3:c.1133T>C (AP4B1)	NP_001240782.1:p.Leu378Pro
NM_001308312.2:c.926T>C (AP4B1)	NP_001295241.1:p.Leu309Pro
NM_006594.5:c.1430T>C (AP4B1)	NP_006585.2:p.Leu477Pro