Canonical Allele Identifier: CA341713995

Gene: AP4B1 AP4B1-AS1

Linked Data

• MyVariant Identifiers: chr1:g.114442985A>C (hg19) ; chr1:g.113900363A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113900363A>C , CM000663.2:g.113900363A>C	GRCh38
NC_000001.10:g.114442985A>C , CM000663.1:g.114442985A>C	GRCh37
NC_000001.9:g.114244508A>C	NCBI36
NG_031901.1:g.9757T>G
NG_057565.1:g.745A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.430T>G (AP4B1)	ENSP00000358577.2:p.Leu144Val
ENST00000369567.6:c.151T>G (AP4B1)	ENSP00000358580.1:p.Leu51Val
ENST00000369571.3:c.655T>G (AP4B1)	ENSP00000358584.3:p.Leu219Val
ENST00000432415.6:c.151T>G (AP4B1)	ENSP00000393622.2:p.Leu51Val
ENST00000460653.2:c.655T>G (AP4B1)	ENSP00000518881.1:p.Leu219Val
ENST00000484201.6:c.430T>G (AP4B1)	ENSP00000518883.1:p.Leu144Val
ENST00000489092.6:c.*323T>G (AP4B1)	ENSP00000518884.1:n.*323T>G
ENST00000489499.6:c.507T>G (AP4B1)	ENSP00000518882.1:p.Tyr169Ter
ENST00000713588.1:c.655T>G (AP4B1)	ENSP00000518880.1:p.Leu219Val
ENST00000713590.1:c.655T>G (AP4B1)	ENSP00000518886.1:p.Leu219Val
ENST00000369569.6:c.655T>G (AP4B1) MANE Select	ENSP00000358582.1:p.Leu219Val
ENST00000256658.8:c.655T>G (AP4B1)	ENSP00000256658.4:p.Leu219Val
ENST00000369564.5:c.430T>G (AP4B1)	ENSP00000358577.1:p.Leu144Val
ENST00000369567.5:c.151T>G (AP4B1)	ENSP00000358580.1:p.Leu51Val
ENST00000369569.5:c.655T>G (AP4B1)	ENSP00000358582.1:p.Leu219Val
ENST00000369571.2:c.655T>G (AP4B1)	ENSP00000358584.2:p.Leu219Val
ENST00000432415.5:c.151T>G (AP4B1)	ENSP00000393622.1:p.Leu51Val
ENST00000472122.1:n.551T>G (AP4B1)
ENST00000484201.5:n.621T>G (AP4B1)
ENST00000489092.5:n.654T>G (AP4B1)
ENST00000489499.5:n.623T>G (AP4B1)
NM_001253852.1:c.655T>G (AP4B1)	NP_001240781.1:p.Leu219Val
NM_001253852.2:c.655T>G (AP4B1)	NP_001240781.1:p.Leu219Val
NM_001253853.1:c.358T>G (AP4B1)	NP_001240782.1:p.Leu120Val
NM_001253853.2:c.358T>G (AP4B1)	NP_001240782.1:p.Leu120Val
NM_001308312.1:c.151T>G (AP4B1)	NP_001295241.1:p.Leu51Val
NM_006594.3:c.655T>G (AP4B1)	NP_006585.2:p.Leu219Val
NM_006594.4:c.655T>G (AP4B1)	NP_006585.2:p.Leu219Val
NR_037864.1:n.860A>C (AP4B1-AS1)
NR_125965.1:n.1028A>C (AP4B1-AS1)
XM_005270381.2:c.655T>G (AP4B1)	XP_005270438.1:p.Leu219Val
XM_005270382.3:c.655T>G (AP4B1)	XP_005270439.1:p.Leu219Val
XM_011540523.1:c.430T>G (AP4B1)	XP_011538825.1:p.Leu144Val
XM_011540524.1:c.430T>G (AP4B1)	XP_011538826.1:p.Leu144Val
XM_011540525.1:c.376T>G (AP4B1)	XP_011538827.1:p.Leu126Val
XM_011540527.1:c.37T>G (AP4B1)	XP_011538829.1:p.Leu13Val
XR_246227.1:n.837T>G (AP4B1)
XR_246228.2:n.837T>G (AP4B1)
XM_011540523.3:c.430T>G (AP4B1)	XP_011538825.1:p.Leu144Val
XM_011540525.3:c.376T>G (AP4B1)	XP_011538827.1:p.Leu126Val
XM_017000089.2:c.655T>G (AP4B1)	XP_016855578.1:p.Leu219Val
XM_017000090.1:c.151T>G (AP4B1)	XP_016855579.1:p.Leu51Val
XM_017000091.2:c.376T>G (AP4B1)	XP_016855580.1:p.Leu126Val
XM_017000092.2:c.-590T>G (AP4B1)	XP_016855581.1:n.-590T>G
XM_017000093.2:c.655T>G (AP4B1)	XP_016855582.1:p.Leu219Val
XM_024452422.1:c.376T>G (AP4B1)	XP_024308190.1:p.Leu126Val
XM_024452423.1:c.655T>G (AP4B1)	XP_024308191.1:p.Leu219Val
XM_024452435.1:c.430T>G (AP4B1)	XP_024308203.1:p.Leu144Val
XM_024452441.1:c.151T>G (AP4B1)	XP_024308209.1:p.Leu51Val
XR_001736928.2:n.857T>G (AP4B1)
XR_001736930.2:n.857T>G (AP4B1)
XR_002958805.1:n.857T>G (AP4B1)
XR_002958806.1:n.857T>G (AP4B1)
XR_002958807.1:n.737T>G (AP4B1)
NM_001253852.3:c.655T>G (AP4B1) MANE Select	NP_001240781.1:p.Leu219Val
NM_001253853.3:c.358T>G (AP4B1)	NP_001240782.1:p.Leu120Val
NM_001308312.2:c.151T>G (AP4B1)	NP_001295241.1:p.Leu51Val
NM_006594.5:c.655T>G (AP4B1)	NP_006585.2:p.Leu219Val