Canonical Allele Identifier: CA341714119

Gene: AP4B1 AP4B1-AS1

Linked Data

• dbSNP Id: rs1279396868
• gnomAD v4: 1-113900397-C-T
• MyVariant Identifiers: chr1:g.114443019C>T (hg19) ; chr1:g.113900397C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113900397C>T , CM000663.2:g.113900397C>T	GRCh38
NC_000001.10:g.114443019C>T , CM000663.1:g.114443019C>T	GRCh37
NC_000001.9:g.114244542C>T	NCBI36
NG_031901.1:g.9723G>A
NG_057565.1:g.779C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.396G>A (AP4B1)	ENSP00000358577.2:p.Met132Ile
ENST00000369567.6:c.117G>A (AP4B1)	ENSP00000358580.1:p.Met39Ile
ENST00000369571.3:c.621G>A (AP4B1)	ENSP00000358584.3:p.Met207Ile
ENST00000432415.6:c.117G>A (AP4B1)	ENSP00000393622.2:p.Met39Ile
ENST00000460653.2:c.621G>A (AP4B1)	ENSP00000518881.1:p.Met207Ile
ENST00000484201.6:c.396G>A (AP4B1)	ENSP00000518883.1:p.Met132Ile
ENST00000489092.6:c.*289G>A (AP4B1)	ENSP00000518884.1:n.*289G>A
ENST00000489499.6:c.473G>A (AP4B1)	ENSP00000518882.1:p.Cys158Tyr
ENST00000713588.1:c.621G>A (AP4B1)	ENSP00000518880.1:p.Met207Ile
ENST00000713590.1:c.621G>A (AP4B1)	ENSP00000518886.1:p.Met207Ile
ENST00000369569.6:c.621G>A (AP4B1) MANE Select	ENSP00000358582.1:p.Met207Ile
ENST00000256658.8:c.621G>A (AP4B1)	ENSP00000256658.4:p.Met207Ile
ENST00000369564.5:c.396G>A (AP4B1)	ENSP00000358577.1:p.Met132Ile
ENST00000369567.5:c.117G>A (AP4B1)	ENSP00000358580.1:p.Met39Ile
ENST00000369569.5:c.621G>A (AP4B1)	ENSP00000358582.1:p.Met207Ile
ENST00000369571.2:c.621G>A (AP4B1)	ENSP00000358584.2:p.Met207Ile
ENST00000432415.5:c.117G>A (AP4B1)	ENSP00000393622.1:p.Met39Ile
ENST00000472122.1:n.517G>A (AP4B1)
ENST00000484201.5:n.587G>A (AP4B1)
ENST00000489092.5:n.620G>A (AP4B1)
ENST00000489499.5:n.589G>A (AP4B1)
NM_001253852.1:c.621G>A (AP4B1)	NP_001240781.1:p.Met207Ile
NM_001253852.2:c.621G>A (AP4B1)	NP_001240781.1:p.Met207Ile
NM_001253853.1:c.324G>A (AP4B1)	NP_001240782.1:p.Met108Ile
NM_001253853.2:c.324G>A (AP4B1)	NP_001240782.1:p.Met108Ile
NM_001308312.1:c.117G>A (AP4B1)	NP_001295241.1:p.Met39Ile
NM_006594.3:c.621G>A (AP4B1)	NP_006585.2:p.Met207Ile
NM_006594.4:c.621G>A (AP4B1)	NP_006585.2:p.Met207Ile
NR_037864.1:n.894C>T (AP4B1-AS1)
NR_125965.1:n.1062C>T (AP4B1-AS1)
XM_005270381.2:c.621G>A (AP4B1)	XP_005270438.1:p.Met207Ile
XM_005270382.3:c.621G>A (AP4B1)	XP_005270439.1:p.Met207Ile
XM_011540523.1:c.396G>A (AP4B1)	XP_011538825.1:p.Met132Ile
XM_011540524.1:c.396G>A (AP4B1)	XP_011538826.1:p.Met132Ile
XM_011540525.1:c.342G>A (AP4B1)	XP_011538827.1:p.Met114Ile
XM_011540527.1:c.3G>A (AP4B1)	XP_011538829.1:p.Met1Ile
XR_246227.1:n.803G>A (AP4B1)
XR_246228.2:n.803G>A (AP4B1)
XM_011540523.3:c.396G>A (AP4B1)	XP_011538825.1:p.Met132Ile
XM_011540525.3:c.342G>A (AP4B1)	XP_011538827.1:p.Met114Ile
XM_017000089.2:c.621G>A (AP4B1)	XP_016855578.1:p.Met207Ile
XM_017000090.1:c.117G>A (AP4B1)	XP_016855579.1:p.Met39Ile
XM_017000091.2:c.342G>A (AP4B1)	XP_016855580.1:p.Met114Ile
XM_017000092.2:c.-624G>A (AP4B1)	XP_016855581.1:n.-624G>A
XM_017000093.2:c.621G>A (AP4B1)	XP_016855582.1:p.Met207Ile
XM_024452422.1:c.342G>A (AP4B1)	XP_024308190.1:p.Met114Ile
XM_024452423.1:c.621G>A (AP4B1)	XP_024308191.1:p.Met207Ile
XM_024452435.1:c.396G>A (AP4B1)	XP_024308203.1:p.Met132Ile
XM_024452441.1:c.117G>A (AP4B1)	XP_024308209.1:p.Met39Ile
XR_001736928.2:n.823G>A (AP4B1)
XR_001736930.2:n.823G>A (AP4B1)
XR_002958805.1:n.823G>A (AP4B1)
XR_002958806.1:n.823G>A (AP4B1)
XR_002958807.1:n.703G>A (AP4B1)
NM_001253852.3:c.621G>A (AP4B1) MANE Select	NP_001240781.1:p.Met207Ile
NM_001253853.3:c.324G>A (AP4B1)	NP_001240782.1:p.Met108Ile
NM_001308312.2:c.117G>A (AP4B1)	NP_001295241.1:p.Met39Ile
NM_006594.5:c.621G>A (AP4B1)	NP_006585.2:p.Met207Ile